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Sem regulus 8230

Manufactured by Hitachi
Sourced in Japan

The SEM Regulus 8230 is a high-resolution scanning electron microscope (SEM) designed for advanced materials analysis. It features a field emission electron gun and a high-resolution objective lens, enabling the visualization of fine details and structures at the nanoscale level. The SEM Regulus 8230 provides high-quality imaging capabilities for a wide range of applications, including materials science, nanotechnology, and life sciences research.

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6 protocols using sem regulus 8230

1

Characterization of Catalytic Powders

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X-ray diffractometer (XRD) patterns were obtained to validate the phase purity and crystallinity of the powders on the XRD equipment (Rigaku Smartlab Beijing Co, Beijing, China). Scanning electron microscope (SEM) images of the prepared catalysts, including energy dispersive X-ray spectroscopy (EDS) capabilities, were measured with an SEM Regulus 8230, Hitachi Co, Tokyo, Japan. The transmission electron microscope (TEM) was used by JEOL JEM-F200 (Tokyo, Japan). The absorption spectra of these powders were tested in a UV-vis spectrophotometer (PerkinElmer Lambda 35, Waltham, MA, USA). X-ray photoelectron spectroscopy (XPS) was carried out with a ESCALAB 250, Thermo-VG Scientific, Waltham, MA, USA to analyze the components and the valence states. The specific surface areas of the samples were tested by Micromeritics ASAP 2460 Brunauer-Emmet-Teller (BET, Shanghai, China) equipment with N2 as the carrier gas. The polarization electric field (P-E) loops and electric-field-induced strain (S-E) were tested in silicone oil at room temperature with 1 Hz frequency using a MultiFerroic II, Radiant technologies Inc., Albuquerque, New Mexico. The sample powders were pressed in a pellet (1 cm diameter and 0.20 mm thick) with Polyvinyl Alcohol (PVA) solution as a binder and then annealed at 600 °C to burn out the PVA binder. The pellets were coated on both sides with Au electrodes.
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2

Ultrasound Effects on Seaweed Surface

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Scanning Electron Microscopy (SEM) was used to investigate the effect of ultrasound on F. vesiculosus surface characteristics. Dried seaweed samples and pellets from the extraction conditions achieving high extraction yields (35 kHz, 50% ethanol, 30 min) and control (no ultrasound, 50% ethanol, 30 min) were collected and prepared as described by Garcia-Vaquero et al. [23 (link)]. The images were recorded using a SEM Regulus 8230 (Hitachi Ltd., Tokyo, Japan).
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3

Characterization of BioTe Nanoparticles

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BioTe with its synthesizer A. pittii D120 was observed by using an SEM Regulus 8230 (Hitachi, Tokyo, Japan). Purified BioTe was analyzed by using an HR-TEM coupled with energy dispersive X-ray spectrometry JEM-F200 (JEOL, Tokyo, Japan). The particle size of BioTe was measured by using a software image J according to images of HR-TEM. To analyze the crystal structure, BioTe solution was concentrated and dried to powder by using a vacuum freeze dryer Heto PowerDry LL3000 (Thermo Fisher Scientific, Waltham, MA, USA). BioTe powder was analyzed by using an XRD Empyrean S3 (Rigaku, Tokyo, Japan). The surface charge of purified BioTe was quantified by using Zetasizer Nano ZS (Malvern Panalytical, Malvern, UK). For the zeta potential analysis, 500 μL BioTe solution was analyzed by using a Zetasizer Nano ZS. A He-Ne laser (633 nm) was used as the light source, the scattering angle was 90 degrees, and the temperature was 28 °C. The experiment was repeated three times.
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4

Visualizing Polymer Membrane Structure

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Scanning electron microscopy imaging was used to visualize morphology and locate where star-like polymer resides within the membrane structure. The pristine membrane was prepared for electron microscopy by the procedure described in [24 (link)]. In short, the pores were first washed with DI water to remove any humectant from the manufacturer and then the water was replaced with ethanol and hexamethyldisilazane (HMDS) by immersing the membrane in solutions of water/ethanol and then ethanol/HMDS with concentration changing from 100% of the first component to 100% of the second one. Samples were dried and mounted to aluminum holders with carbon tape and then coated with platinum for 2 min using an Anatech Hummer 6.5 sputter coater (Sparks, NV, USA). The Pt coating thickness was 4 nm. Micrographs of the membrane surfaces were taken using a Hitachi Regulus 8230 SEM (Tokyo, Japan) at an accelerating voltage of 20 kV.
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5

Characterization of Spherical Nanoparticle Explosive Columns

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Material: DNAN, purity greater than 99%, Liaoning Liaoyang Special Chemical Co., Ltd (Liaoning, China). Ordinary NQ, spherical NQ (d50 = 500 μm) and spherical NQ with particle gradation (d50 = 1000, 200, 30 μm), industrial grade, Liaoning Liaoyang Special Chemical Co., Ltd. The microstructure features of the sample were characterized by a Regulus-8230 SEM (scanning electron microscope, Hitachi, Tokyo, Japan), and the results are shown in Figure 1. The slow cook-off sample column is spherical NQ-based melt-cast explosive, and the formula (mass fraction) is 75%NQ/25%DNAN. Due to its low density and poor fluidity, ordinary NQ tends to form agglomerates during melting and is difficult to charge and form. The content in melt-cast explosives is generally less than 50%. Therefore, ordinary NQ explosive columns with a solid content of 75% have not been cast this time.
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6

Comprehensive Characterization of Biochar

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The FT-IR spectra of the as-fabricated biochar were collected on a Spectrum Two L1600300 spectrometer (PerkinElmer Inc., Waltham, MA, USA). The Raman spectra of the biochar were recorded on a DXR Raman Microscope Laser Raman spectrometer (Thermo Fisher Scientific Inc., Waltham, MA, USA). The XRD patterns of all samples were performed on a MiniFlex600 diffractometer (Rigaku Corporation, Tokyo, Japan) in a range of 10° to 80°. The surface chemical compositions of the as-fabricated biochar were determined by an Escalab 250Xi XPS (Thermo Fisher Scientific Inc., Waltham, MA, USA) characterization. The STA-449F3 thermal balance analyzer (NETZSCH Inc., Selb, Bavaria, Germany) was used to obtain the TG curves of the as-fabricated biochar. The surface morphology of biochars were recorded by SEM images on a REGULUS 8230 SEM (Hitachi Co., Tokyo, Japan) and TEM images on a FEI Tecnai G2 F20-TWIN TEM (FEI Co., Hillsboro, OR, USA). The micromeritics TRISTAR II3020 surface area analyzer (Micromeritics Instrument, Norcross, GA, USA) was used to determine the BET surface area of biochars. Zeta potentials of different pH solutions were recorded on a Zetasizer Nano ZS90 zeta potential analyzer (Malvern Panalytical, Malvern, UK). The total amount of heavy metal ions was determined by an ICP-OES (ICAP7400, BRE0002948, Thermo-Fisher Scientific Inc., Waltham, MA, USA).
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