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D max 2550 pc xrd

Manufactured by Rigaku
Sourced in Japan

The D/max-2550 PC XRD is a X-ray diffractometer designed for powder and thin-film analysis. It utilizes a copper X-ray source and a proportional counter detector to measure the diffraction patterns of crystalline materials. The instrument is controlled by a PC and provides data collection and analysis capabilities.

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6 protocols using d max 2550 pc xrd

1

X-ray Diffraction Analysis of Nylon 6,6 Fibers

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The crystal structures of the neat and the salt-confined nylon 6,6 fibres are investigated using an X-ray polycrystal diffractometer (XRD)—D/max-2550 PC, manufactured by Rigaku (Tokyo, Japan).
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2

Crystallinity Analysis of Polyester Fabrics

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An XRD D/Max-2550 PC (RIGAKU Co., Ltd., Tokyo, Japan) was used to measure the degree of crystallinity of fabrics, which describes the molecular structure of the polyester filaments. Damage to these molecular structures would alter the mechanical characteristics of the fabric.
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3

Characterizing Zinc Oxide-Zinc Sulfide Core-Shell Nanoparticles

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A field-emission scanning electron microscope (FE-SEM, Quanta 200 FEG) was used to evaluate the morphology and size of the CSNPs. An aqueous dispersion of Uf-gel-ZnO-ZnS CSNPs was poured on a silicon substrate and dried at 37°C to eliminate moisture. Then, the samples were evaluated using FE-SEM operating at a 5 kV accelerated voltage. For high-resolution transmission electron microscopy (HR-TEM, JEOL JEM-2100), a diluted suspension of 5 μL Uf-gel-ZnO-ZnS CSNP was deposited on a carbon-coated copper grid and dried at 37°C. Then, the samples were analyzed with an accelerating voltage of 200 kV. The crystallinity of the formed ZnO-ZnS CSNPs was examined using the XRD technique (D/max-2550 PC XRD, Rigaku, Japan). The Uf-gel-ZnO-ZnS CSNPs are blended with the powder form of KBr and formed as a pellet for the acquisition of the FTIR spectrum (Nicolet 6700), scanned in transmission mode at 4000-400 cm−1 range.
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4

Multimodal Characterization of Samples

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The morphology of as‐prepared samples were investigated by SEM (Hitachi, S‐4800) and TEM (JEM‐2100F). XRD were conducted by a D/max‐2550 PC XRD (Rigaku, CuKα radiation). In situ TEM experiments were performed in TEM with the TEM‐STM holder of Nanofactory (Gothenburg, Sweden). XPS data were obtained using XPS (ESCALAB 250Xi, Thermo Scientific, USA). The Raman spectra were measured by InVia Reflex (Renishaw).
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5

Characterization of Carboxymethyl Cellulose Nanoflowers

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A high-resolution transmission electron microscope (HR-TEM, Hitachi/HF-3300) was utilized to determine the morphology and composition of NFs. The surface morphology and structure of CMC NFs were assessed using a high-resolution field-emission SEM (HR-FE-SEM, Hitachi/SU8020). Then, the absorption spectrum of FA–CMC NFs was acquired with a nanodrop (DS-11+, DeNovix, USA) spectrophotometer, in which the absorbance of the surface-modified NFs was studied as a function of wavelength. The X-ray diffraction (XRD, D/max-2550 PC XRD, Rigaku) technique was used to determine the crystallinity of CMC NFs at 2θ values of 10–80°. The purity and surface oxidation were demonstrated using an X-ray photoelectron spectrometer (XPS) in the fabricated CMC NFs (Thermo Scientific/ESCALAB 250Xi). The Raman spectrum of the nanoflower was obtained using a inVia-Reflex micro-Raman spectroscopy (Thermo Scientific/Nicolet Almega XR) system using a laser with a wavelength of 532 nm.
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6

Comprehensive Material Characterization Protocol

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The morphology of as-prepared samples was investigated by scanning electron microscopy (SEM, Hitachi S-4800) and transmission electron microscopy (TEM, JEM-2100F). X-ray diffraction (XRD) patterns were collected by a D/max-2550 PC XRD (Rigaku, CuKα radiation). X-ray photoelectron spectroscopy (XPS) spectra were obtained using Escalab 250Xi. The nitrogen adsorption/desorption isotherms were measured by ASAP 2020 instrument and the specific area was calculated by the BET method. Thermogravimetric analysis (TGA) was conducted in N2 using Discovery TGA Q5000IR from 50 to 500 °C at a heating rate of 5 °C min−1. The Raman spectra were measured by InVia Reflex (Renishaw) with a 532 nm laser.
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