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34 protocols using x ray diffractometer

1

Comprehensive Characterization of Silver Nanoparticles

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UV–visible spectroscopy (UV–vis) spectra of the prepared Ag-NPs and Ag-NC were measured on V-630 UV–vis spectrophotometer (Jasco, Japan) in the range of 300–700 nm. The Ag-NC and its component were characterized using FT-IR spectrometer (Nicolet Impact-400 FT-IR spectrophotometer) in the range of 400–4000 cm−1 using KBr method (0.002 g sample was grinded with 0.98 g KBr) using Spectrum Two IR Spectrometer – Perk in Elmer, Inc., Shelton, USA. The X-Ray diffraction (XRD) of Ag-NC and its component were investigated on a Diano X-ray diffractometer using Cu-Kα radiation source energized at 45 kV and a Philips X-ray diffractometer (PW 1930 generator, PW 1820 goniometer) with Cu-Kα radiation source (λ = 0.15418 nm) XRD Model diffractometer, Shimadzu 7000, Japan. The topographical study was carried out using scanning electron microscopy (SEM) with energy dispersive electron spectroscopy (EDX) Model FEI IN SPECTS Company, Philips, Holland, environmental scanning without coating. The surface morphology of Ag-NPs and Ag-NC was carried out using JEOL 1010 transmission electron microscopy (TEM), Model JEM2010, Japan. The samples were processed according to (Shehabeldine et al. 2021a (link); Elbahnasawy et al. 2021a ).
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2

Characterization of AuNPs and CS-AuNPs

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The Malvern Zeta sizer Nano ZS system (Malvern Instruments Ltd., Worcestershire, UK) was used to assess the zeta potential of AuNPs and CS-AuNPs at 25 °C. The XRD patterns of AuNPs and CS-AuNPs were obtained with a Diano X-ray diffractometer and a Philips X-ray diffractometer at 45 kV, 4/min, and a scanning range of 5 ~ 80. The UV-visible absorption spectra of AuNPs and CS-AuNPs were measured at ambient temperature using a spectrophotometer (JENWAY 6305 Stone, UK) within the 300–800 nm wavelength range.
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3

X-ray Diffraction Analysis of GBP Formulations

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The X-ray diffraction study was carried out to characterize the physical form of GBP in samples of optimized formula. The physical state of GBP in the various preparations were recorded at room temperature on X-ray diffractometer (Philips, USA) with mono-chromator Cu radiation (1.542 Ǻ), at 40 kV, 35 mA. The diffractometer was equipped with a 2θ compensating slit, and was calibrated for accuracy of peak positions with silicon pellet. Samples were subjected to X-ray powder diffraction analysis in continuous mode with a step size of 0.02° and step time of 1 s over an angular range of 2–60°2θ.
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4

Characterization of Nanomaterials via Spectroscopy

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The results were acquired by an FS5 spectrofluorometer (Edinburgh, UK) with a 150 W xenon lamp source for excitation. Also, with 1-cm quartz cell and connected to Fluoracle® software. The slit widths were set to 2 nm and the scanning speed 1000 nm/min. The dynamic light scattering measurements (DLS) were scanned by Zetasizer Red badge instrument of ZEN 3600 (Malvern, UK). MFMI-100A (MED Future) Microwave instrument (2450 MHz, 0- 1000 W) was designed for catalyzing organic synthesis and solvent extraction. Magnetic and Mechanical stirring- IR Temperature Sensor (0–300'C). Fourier-transform infrared (FTIR) Germany. pH-meter (China). The powder X-ray diffraction (PXRD) was scanned by Philips X-ray diffractometer. High-resolution transmission electron microscope (HR-TEM) images were captured via JEOL JEM-100CX II unit tungsten EM filament 120 (USA).
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5

Comprehensive Materials Characterization

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The fabricated products were analyzed using an X-ray diffractometer (XRD, Philips X-ray diffractometer with Cu Kα radiation at λ = 1.541 Å) to obtain crystallographic information. Morphology and structural characteristics were studied using a field-emission scanning electron microscope (FESEM, JEOL FEG JSM 7001F) and a transmission electron microscope (TEM, Phillips FEG CM300), respectively. The elements were analyzed by energy-dispersive X-ray spectroscopy (EDX, Oxford Instruments). The absorption spectra of photocatalysts were obtained using a UV-visible spectrophotometer (UV-vis, Shimadzu UV-3600).
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6

Phase Analysis of Synthesized Powder

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X-ray diffractometer (Philips Netherlands Company with Cukα radiation, wavelength 1.54 A°) was used for phase analysis of the synthesized powder and the SCA surfaces of the membranes26 (link).
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7

X-ray Diffraction Analysis of Crystal Forms

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The crystal form of raw LE, LE-NPs, and Poloxamer 188 was detected and analyzed by an X-ray diffractometer (Philips, Amsterdam, the Netherlands). The sample was irradiated with a Cu target tube and was detected at 40 kV and 30 mA at 3°<2θ<60°.
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8

Perovskite Film Characterization by XRD

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XRD spectra of the perovskite films were obtained by a Philips X-ray diffractometer with CuKα radiation.
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9

Characterization of Zeolite 13X Adsorbents

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XRD
measurement of all of the adsorbents was done using a Philips X-ray
diffractometer (model: PW 1729) using Cu Kα radiation and PC-APD
diffraction software. The XRD pattern of each sample was measured
using 10% α-Al2O3 as the internal standard.
Major crystallinity changes were monitored using a Bruker D-8 advance
X-ray powder diffractometer without using any internal standard or
specific sample pretreatment method.
The BET surface area, pore
volume, average pore diameter, and textural properties of molecular
sieve zeolite 13X (NaX) and ion-exchanged zeolite 13X were determined
by N2 adsorption–desorption isotherms at 77 K using
a surface area analyzer ASAP 2020 (M/S Micromeritics). The adsorbents
were degassed at 573 K using vacuum atmosphere for >12 h prior
to
generating adsorption isotherms. To estimate the percentage loading
of different metal ions, metal analysis of the parent zeolite 13X
and ion-exchanged zeolite 13X was done using an inductively coupled
plasma-optical emission spectrometer (ICP-OES).
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10

Powder XRD Analysis of Drug-Excipient Interactions

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An X-ray diffractometer (Philips, UK) was used to record the powder XRD of TC, PEG-6000, β-CD, TC+PEG, TC+β-CD, TC+PEG-6000+β-CD, and solid dispersions. The scanning rate used was 5/min, and the diffraction angle (2θ) was 0–70 [21 (link)].
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