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D max rc x ray diffractometer

Manufactured by Rigaku

The D/MAX-RC X-ray diffractometer is a versatile laboratory instrument designed for the analysis of crystalline materials. It utilizes X-ray diffraction technology to provide information about the atomic and molecular structure of a wide range of samples. The core function of this equipment is to record and analyze the diffraction pattern generated when a sample is exposed to an X-ray beam, enabling the identification and characterization of crystalline phases present in the material.

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2 protocols using d max rc x ray diffractometer

1

Comprehensive Characterization of As-Prepared Samples

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Powder X-ray diffraction (XRD) analysis was performed using a Rigaku D/MAX-RC X-ray diffractometer to identify the crystalline phases of the as-prepared samples. The morphologies of the as-prepared samples were observed on a transmission electron microscope (TEM, JEOL, JEM-2100, 200 kV) and field emission scanning electron microscope (FESEM, Hitachi, S-4800, 15 kV). Fourier transform infrared (FT-IR) spectra were recorded on a PerkinElmer Spectrum One spectrophotometer using KBr disks in the range of 500 to 4000 cm−1. X-ray photoelectron spectroscopy (XPS) measurements were carried out on a Kratos Axis Ultra-DLD spectrometer equipped with monochromatic Al–K radiation (hv = 1486.6 eV). The carbonaceous C 1s line (284.6 eV) served as the reference to calibrate the binding energies (BEs). Thermogravimetric (TG) analysis was performed using a PerkinElmer Pyris 1 TGA thermo balance. In the TG experiment, the as-prepared samples were heated from 30 °C to 700 °C at 10 °C min−1 in an air atmosphere. The zeta potential of the as-prepared dispersions was investigated using a Brookhaven 90 Plus PALS analyzer.
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2

Synthesizing Piezoelectric Ceramic Compositions

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The system of 0.985(K1/2Na1/2)O3-0.015Ba(Cu1/3Nb2/3)O3 was synthesized from the oxides of >99% purity by the conventional solid-state route. The powders of K2CO3, Na2CO3, Nb2O5, BaCO3, and CuO (all obtained from Sigma Aldrich) were mixed for 6–48 h in a polypropylene jar with zirconia balls. This mixture of powders was dried and calcined at the temperature range of 800–950 oC for 3 h. Calcined powders were milled for 6–48 h, dried and pressed into disks under the pressure of 10 MPa and sintered in the range of 1070~1120 oC for 2–10 h. The giant grain was obtained when the powders were ball-milled for 6–18 h (both 1st and 2nd ball-milling processes). The crystal structure of specimens was examined using Rigaku D/max-RC X-ray diffractometer. The microstructure was observed under a scanning electron microscope (SEM, JSM-5800; JEOL CO., Tokyo, Japan). The samples were poled in silicone oil at 120 oC by applying a dc field of 2–4 kV/mm for 30 min. All the electrical measurements were conducted after aging the samples for 24 h. The piezoelectric and dielectric properties were determined using a piezo d33 meter (Micro-Epsilon Channel Product DT-3300) and an impedance analyzer (4294A, Agilent Technologies, Santa Clara, CA, USA).
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