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Nicolet 370 ft ir spectrometer

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Nicolet 370 FT/IR spectrometer is a versatile laboratory instrument designed for molecular analysis. It utilizes Fourier transform infrared (FT-IR) spectroscopy to identify and characterize a wide range of organic and inorganic compounds. The core function of the Nicolet 370 FT/IR spectrometer is to collect and analyze infrared absorption spectra, providing detailed information about the molecular structure and composition of samples.

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4 protocols using nicolet 370 ft ir spectrometer

1

Comprehensive Characterization of Materials

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Fourier transform infrared (FT-IR) spectra of samples were measured using Nicolet 370 FT-IR spectrometer (Thermo Nicolet Corporation, American, Madison, WI, USA). Nitrogen adsorption (Brunauer-Elmett-Teller, BET) was performed with a Surface Area and Pore Size Analyzer (Micromeritics TriStar3000) at 77 K/1 bar. Thermogravimetric analysis (TGA) was conducted on a SII TG/DTA 6300 thermogravimetric analyzer. X-ray diffraction (XRD) spectra were collected on an Ultima IV X-ray diffractometer (Japan Science Co., Ltd. Tokyo, Japan) using copper Kα radiation at a voltage of 30 kV and 20 mA over the 2θ range of 5–90°. The morphology was analyzed using a field emission scanning electron microscope (SEM) supplied by ZEISS (Sigma 300, Cambridge, UK). Atomic absorption spectroscopy (AAS, Shimadzuatomic absorption spectrometer, Kyoto, Japan) was employed to analyze Zn2+ concentration in the adsorption investigation.
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2

Green-Synthesized Multifunctional Nanocomposites

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High-purity chemicals were purchased from Merck and Aldrich chemical companies. X-ray diffraction (XRD) measurements were carried out using a Philips powder diffractometer type PW 1373 goniometer with scanning rate of 2° min−1 in the 2θ range from 0° to 90°. UV-visible spectra for analysis were recorded on a double-beam spectrophotometer (Super Aquarius) to monitor the SPR signals of the nanoparticles. The morphology, particle dispersion and chemical composition of the prepared nanostructures were investigated by fast emission scanning electron microscopy (FE-SEM) (Quanta 450) equipped with EDS (energy dispersive X-ray spectroscopy). FT-IR spectra were recorded on a Nicolet 370 FT/IR spectrometer (Thermo Nicolet, USA) using pressed KBr pellets. The antibacterial activity of the green-synthesized ZnO@CuO@iron ore NCs was studied using the disc diffusion method via Muller–Hinton media and by using chloramphenicol as positive control. The Pseudomonas aureus, Staphylococcus aureus and Escherichia coli were obtained from the Department of Biology, Soran University in KRG, Iraq.
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3

Synthesis and Characterization of Cu/MgO Nanocomposites

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All materials with commercial reagent grade were obtained from the Merck and Aldrich companies and used without further purification. FT-IR spectra were recorded on a Nicolet 370 FT/IR spectrometer (Thermo Nicolet, USA) using pressed KBr pellets. The formation of nanoparticles was recorded by UV-visible spectral analysis on a double-beam spectrophotometer (Hitachi, U-2900). The shape and size of the Cu/MgO nanocomposite were identified by transmission electron microscope (TEM) using a Philips EM208 microscope operating at an accelerating voltage of 90 kV. Field emission scanning electron microscopy (FE-SEM) was performed on a cam scan MV2300. EDS (energy dispersive X-ray spectroscopy) was utilized for chemical analysis of prepared nanostructures. X-ray diffraction (XRD) mensuration were carried out using a Philips powder diffractometer type PW 1373 goniometer (Cu Kα = 1.5406 Å). The scanning rate was 2° min−1 in the 2θ range from 10 to 90°.
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4

Characterization of Fe3O4@SiO2-phenyl-tetrazole

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All materials of commercial reagent grade were purchased from the Merck and Aldrich companies and used without further purification. FT-IR spectra were recorded on a Nicolet 370 FT/IR spectrometer (Thermo Nicolet, USA) using pressed KBr pellets. X-ray diffraction (XRD) measurements were carried out with a Philips powder diffractometer type PW 1373 goniometer. It was equipped with a graphite monochromator crystal. The X-ray wavelength was 1.5405 Å and the diffraction patterns were recorded in the 2θ range (10–80) with a scanning speed of 2° min−1. TEM images were taken using a Philips EM208 transmission electron microscope with an accelerating voltage of 90 kV. Scanning electron microscopy (SEM) of the {Fe3O4@SiO2@(CH2)35-phenyl-1H-tetrazole-SO3H/HCl} was performed on a Cam scan MV2300. The chemical compositions of the synthesized catalyst were determined by EDS (energy dispersive X-ray spectroscopy) performed in SEM. Thermal analysis (TG-DTG) was carried out using an STA 1500 Rheometric Scientific (England). The flow rate of air was 120 mL min−1 and the ramping rate of the sample was 2 °C min−1. VSM measurements were recorded using a SQUID magnetometer at 298 K (Quantum Design MPMS XL). Melting points were taken in open capillaries using BUCHI 510 melting point apparatus and are uncorrected.
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