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Win ir spectrometer

Manufactured by Bio-Rad
Sourced in United Kingdom

The Win-IR Spectrometer is a laboratory instrument used for performing infrared (IR) spectroscopy. It is designed to analyze the absorption and transmission of infrared radiation by samples, providing information about the chemical composition and molecular structure of the analyzed materials.

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4 protocols using win ir spectrometer

1

Characterization of Gadolinium Phosphate Nanostructures

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The crystal phase was analyzed by powder X-ray diffraction (XRD; Bruker Co., Bremen, Germany) on a D8 Advance diffractometer using Cu Kα radiation (λ = 0.154 Å). The morphology, structure and size of the samples were determined by field-emission scanning electron microscopy (FESEM; Philips XL30 ESEM FEG, Japan) and transmission electron microscopy (TEM; FEI Tecnai G2 S-Twin, München, Germany). The elemental compositions were analyzed by energy-dispersive X-ray energy spectrometry (EDX; Philips, XL-30 W/TMP, Konan, Japan). Fourier transform infrared spectrometry (FT-IR, Bio-Rad Win-IR Spectrometer, Watford, UK) was recorded in the range of 400–4000 cm−1 using the attenuated total reflection (ATR) mode and the KBr slice method. Atom force microscopy (AFM) images were acquired by Bruker’s Dimension Icon and Multimode-V AFM. The amounts of GdPO4·H2O, GdPO4·H2O@SiO2, GdPO4·H2O@SiO2–APS, and PBLG-g-GdPO4·H2O were determined by thermogravimetric analysis (TGA, TA Instruments TGA500, New Castle, DE, USA) in air at a heating rate of 10 °C/min from 25 °C to 800 °C.
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2

Characterization of PEEK Film Microstructure

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Fourier-transform infrared spectroscopy (FT-IR, Bio-Rad Win-IR Spectrometer, Watford, UK) spectra were recorded using the KBr slice method. An environmental scanning electron microscope (SEM, XL30 FEG, Philips) was used to observe the microstructure of PEEK films. Energy dispersive X-ray spectrometry (EDX) (XL-30W/TMP, Philips, Japan) was employed to analyze the elemental composition. For each sample, the size of 200 pores from five different SEM images were measured using Image J software to calculate micro-pore size distribution. N2 adsorption desorption measurements were carried out at 77K to characterize meso-pore properties. The specific surface areas of the samples were calculated by the BET (Brumauer - Emmett - Teller) method with N2 adsorption data.
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3

Synthesis and Characterization of EGCG-Selenium Nanoparticles

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EGCG-Se NP were prepared as previously described (Zhang et al., 2010 (link)). Briefly, 2.75 g of EGCG (6 mmol) and 0.129 g of selenious acid (1 mmol) were added to 4 ml of 75% ethanol aqueous solution and stirred to completely dissolve. Then, 10 ml of sodium ascorbate solution (5 M) were dripped into the mixture, and the reaction took place overnight in a nitrogen atmosphere. After dialysis and lyophilization, EGCG-Se NP was obtained.
The size distribution of EGCG-Se NP was assessed with a ZEN3600 instrument (Malvern, Worcestershire, United Kingdom). Transmission electron microscopy (TEM) images were obtained with a JEM-1011 microscope (JEOL, Tokyo, Japan) at an accelerating voltage of 100 kV. X-ray photoelectron spectroscopy was performed with an X-ray surface photoelectron spectrometer (Thermo ESCALAB 250, United Kingdom). The Fourier transform infrared spectra (FT-IR) and ultraviolet-visible absorption spectra were acquired utilizing a Win-IR spectrometer (Bio-Rad, Hercules, CA) and a UV-Lambda365 spectrophotometer (PerkinElmer, Waltham, MA), respectively.
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4

Fourier Transform Infrared Spectroscopy

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Fourier transform infrared (FTIR, Bio-Rad Win-IR spectrometer, UK) spectrometry was used to detect chemical groups. The FTIR spectra were obtained in the wavelength range of 400–4000 cm−1 with a resolution of 4 cm−1.
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