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Xrd 6000

Manufactured by Rigaku
Sourced in Japan

The XRD-6000 is a versatile X-ray diffractometer designed for a wide range of applications in materials analysis. It is capable of performing high-resolution X-ray diffraction measurements to identify and characterize crystalline materials.

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3 protocols using xrd 6000

1

Comprehensive Catalyst Characterization

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The morphologies and elemental mapping of series catalysts were observed by scanning electron microscopy (SEM, Zeiss, sigma500, Jena, Germany) with an Oxford Ultim Max Large Area SDD EDS detector. The size of catalysts was measured by a laser particle size analyzer (Malvern, MS-2000, Malvern, UK). The crystallographic structures of catalysts were characterized by a high-resolution transmission electron microscope (HRTEM, JEM-2100, Tokyo, Japan) and X-ray diffraction (XRD, Rigaku Corporation, XRD-6000, Tokyo, Japan). The specific surface area and pore size distribution of samples were analyzed by Brunauer–Emmett–Teller (BET) and Barrett–Joyner–Halenda (BJH) methods, respectively. A Fourier-transform infrared spectrophotometer (FT-IR, American Nicolet Corp. Model 170-SX, Green Bay, WI, USA) was used to investigate the chemical structures of the catalyst. X-ray photoelectron spectroscopy (XPS, Thermo Fisher Scientific, ESCALAB250Xi, Waltham, MA, USA) was utilized to study the surface chemical composition of catalysts. To study the catalytic mechanism of CDM, an electron paramagnetic resonance spectrometer (Bruker ELEXSYS E500, Karlsruhe, Germany) was used to obtain the EPR signals. The leaching of Cu and Mn in wastewater was detected by an inductively coupled plasma spectrometer (Agilent 5800 ICP-OES, Santa Clara, CA, USA).
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2

Structural Characterization of MM'-CNT@CNF Catalysts

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Structural characterization was done by collecting Powder X-ray diffraction (PXRD) data in the scan range of 0–70° 2θ using Rigaku XRD-6000 (Cu Kα, 40 kV, 30 mA). Thermo Scientific™ Nexsa™ X-ray Photoelectron Spectrometer (XPS) was performed for binding energy analysis and to estimate the nitrogen content. The sizes, morphologies, and elemental analysis of the fabricated catalysts were studied by scanning electron microscopy (SEM) using QFEG 200 Cryo ESEM equipped with energy-dispersive X-ray spectroscopy (EDX). Detailed structural investigation was done by transmission electron microscopy (TEM) analysis with Titan Analytical 80–300 ST TEM. Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) was used to calculate the metallic content in the prepared MM′-CNT@CNF.
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3

Characterizing CoFe-LDH/MoS2 Catalyst Structure

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The crystallinities of CoFe-LDH, MoS2, and CoFe-LDH/MoS2 were determined using X-ray powder diffractometry (XRD). Powder XRD measurements were performed on a Rigaku XRD- 6000 diffractometer with Cu Ka radiation (λ = 0.15418 nm) at 40 kV and 40 mA. The scanning rate was set at 5° min−1, and the 2θ angle ranged from 5° to 80°. The morphology of the CoFe-LDH/MoS2 catalyst was investigated using a scanning electron microscope (SEM, Zeiss Sigma 300, Germany) and high resolution transmission electron microscope (HRTEM, FEI Tecnai G2 F30, USA). The specific surface areas of the samples were recorded by the Brunner–Emmett–Teller (BET) technique (ASAP2460, USA). The catalyst surface’s functional groups were identified using Fourier transform infrared spectroscopy (FT-IR, Thermo Scientific, Nicolet iS5, USA). X-ray photoelectron spectroscopy (XPS) information was obtained using a spectrometer (Thermo Escalab 250Xi, USA). The reactive oxygen species were monitored by electron paramagnetic resonance (EPR, Bruker EMX Plus, USA) spectrometer, and DMPO and TEMP were used as a trap for ·O2, ·OH and 1O2. Furthermore, HPLC-MS (Shimadzu, LC-6AD, Japan) equipped with a Waters XTerra C18 column was used to investigate the intermediates during the degradation of TCH and its possible degradation pathways.
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