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Iraffinity 1s spectrophotometer

Manufactured by Shimadzu
Sourced in Japan

The IRAffinity-1S is a Fourier Transform Infrared (FT-IR) spectrophotometer manufactured by Shimadzu. It is designed to analyze the molecular composition and structure of various samples by detecting their infrared absorption spectrum. The IRAffinity-1S provides high-quality data and accurate results, making it a reliable tool for applications in various fields such as materials science, chemistry, and research.

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23 protocols using iraffinity 1s spectrophotometer

1

Synthesis and UV-vis Analysis of Hydrazine Derivatives

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The reagents and the solvents used for the synthesis and UV-vis studies were of analytical and spectroscopic grade. Phenyl hydrazine, hydrazine hydrate, ethyl 2-chloroacetate and ethyl acetoacetate were purchased from Spectrochem Pvt. Ltd and were used without further purification. All the amino acids used in UV-vis studies were purchased from Sigma Aldrich and Spectrochem Pvt Ltd. 1H and 13C NMR were recorded at room temperature on a JNM-EXCP 400 (JEOL, USA) spectrometer using TMS as an internal standard and the chemical shifts are reported in parts per million (ppm). FTIR data was recorded using a Shimadzu IR Affinity 1S Spectrophotometer. The crude products were purified using column chromatography (silica gel 100–200 mesh) and methanol–chloroform as the solvent system. UV-vis experiments were performed on a Carey Series UV-vis spectrophotometer using a 1 cm quartz cuvette. All experiments were performed in compliance with the policy statement on ethical considerations involved in research on human subjects (ICMR, 1980). These experiments were approved by the departmental research committee of University of Delhi. The blood sample of a healthy volunteer was procured from a local pathology lab and arginine granule supplements were commercially available in the market. The donor provided informed consent in accordance with the guidelines of the institution.
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2

FTIR Analysis of Alcohols and Carboxylic Acids

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Alcohols (Aldrich, St Louis, MO, USA) and carboxylic acids (Aldrich, St Louis, MO, USA) with different molecular weight were used as target samples. Alcohols were ethanol and n-butanol and n-hexanol, whereas carboxylic acids were formic acid, acetic acid and citric acid. Deionized water was used in all cases. These compounds were selected by practical importance of main functional groups associated with them: carboxylic acid (—COOH), carbonyl (—C<svg xmlns="http://www.w3.org/2000/svg" version="1.0" width="20.666667pt" height="16.000000pt" viewBox="0 0 20.666667 16.000000" preserveAspectRatio="xMidYMid meet"><metadata>
Created by potrace 1.16, written by Peter Selinger 2001-2019
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O) and hydroxyl (—OH). All reagents were analytical grade. Samples were analyzed by FTIR spectroscopy by attenuated total reflectance (ATR-FTIR) using an IRAffinity-1S spectrophotometer from Shimadzu Co (Kyoto, Japan).
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3

Comprehensive Characterization of Nanomaterials

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UV-vis absorption spectra were measured via a Shimadzu UV-2700 UV-vis spectrophotometer. The transmission electron microscopy (TEM) images were obtained on a ThermoFisher Tecnai G2 Spirit TEM microscope. The Fourier transform infrared (FTIR) spectra were recorded on a Shimadzu IRAffinity-1S spectrophotometer. The dynamic light scattering (DLS) images were generated on a Malvern ZEN3700 DLS and Zeta Sizer. The Raman spectra were measured by a Renishaw's inVia Raman spectrometer.
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4

FTIR Analysis of Molecular Interactions

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FTIR spectra were obtained to understand the molecular interactions and functional group characterization. The FTIR spectra were obtained using an IRAffinity-1S spectrophotometer (Shimadzu, Kyoto, Japan) in ATR-FTIR mode. All spectra were recorded with the resolution of 4 cm−1 in the range of 400–4000 cm−1 with 20 scans.
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5

FT-IR Characterization of Sample

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The sample was characterized by means of IR spectrophotometry. The Fourier transformed infrared (FT-IR) spectra of the sample were recorded with a Shimadzu IR Affinity-1S spectrophotometer (Shimadzu, Duisburg, Germany) in the range of 400–4000 cm−1, using the method of potassium bromide pellets, with a resolution of 4 cm−1.
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6

Detailed Characterization of Molecular Compounds

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All solvents and chemicals were
purchased from commercial suppliers (Aldrich, Alfa Aesar, and TCI
Chemicals) and used as received. Solvents were purified with appropriate
drying agents when required. All moisture-sensitive reactions were
carried out under a nitrogen atmosphere. The UV–vis absorption
spectra were recorded with UV–vis spectrophotometer (SHIMADZU
01174) with BaSO4 as a reference, equipped with a diffuse
reflectance accessory. Fourier transformed infrared (FTIR) measurement
was carried out with a Shimadzu IRAffinity-1S spectrophotometer with
KBr pellets. HRMS was recorded using a fast-atom bombardment double-focusing
magnetic sector mass spectrometer and the electron impact ionization
technique (magnetic sector–electric sector double-focusing
mass analyzer). 1H NMR (500 MHz) and 13C NMR
(200 MHz) spectra were analyzed on the NMR spectrometer. EPR experiments
were carried out using the Bruker EMX plus X-Band EPR spectrometer.
Powder X-ray diffraction (PXRD) patterns were recorded on a Philips
PW3040/60 high-resolution diffractometer.
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7

FT-IR Analysis of Microplastic Samples

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About 20% of the isolated items were randomly selected according to their morphological prevalence and analyzed for the chemical identification of the constituent polymer by Fourier-transformed infrared (FT-IR) spectroscopy. Items were sampled from the filter surface under the stereomicroscope using a small tweezers or a little brush, washed in double-filtered deionized water and stored in glass vials. FT-IR analysis was performed using an IRAffinity-1S spectrophotometer (Shimadzu, Japan) equipped with a sealed and desiccated interferometer, a DLATGS (Deuterated Triglycine Sulphate Doped with L-Alanine) detector and a Specac Quest ATR accessory (Specac Ltd, London, England). The IR spectra of the selected items were recorded in the range from 4000 cm-1 to 400 cm-1 (45 scans, 4 cm–1 resolution) with Happ– Genzel apodization and elaborated using Lab Solution IR v. 2.16 software. The IR spectra of the identified items was compared with Shimadzu ATR polymers Library and an index of at least 70% match was considered acceptable. A background reading was collected before each test and two readings were taken from each analyzed item.
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8

Characterization of Doped Mesoporous Bioactive Glass Nanoparticles

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Retrieved particles were subjected to further characterization of morphology and elemental composition. To determine the morphology, scanning electron microscopy (FESEM, Auriga Crossbeam, Carl Zeiss Microscopy, GmbH, Jena, Germany) was employed. Obtained SEM micrographs were imported into an image analysis software (ImageJ, NIH, United States) to estimate the average particle size and distribution (n = 30). Li content in the doped MBGNs particles was also assessed by inductively coupled plasma optical emission spectroscopy (ICP-OES). Molecular analysis of the TCS and MBGN powder particles was conducted by Fourier transform infrared spectroscopy (FTIR) (SHIMADZU, IRAffinity-1S spectrophotometer, Shimadzu Corp, Tokyo, Japan). 40 scans at a resolution of 4 cm-1 in the 400 to 4000 cm-1 wavelength range were captured in absorbance mode. Structural analysis of the powders was done by x-ray diffraction (XRD) (Miniflex 600 HR, Rigaku, Japan) using 40 kV copper K-α radiation. The data were obtained in the 2Ɵ range, between 10 and 70. A step size of 0.020 and speed of 4o per minute were employed. Both FTIR and XRD data were normalized to 0–1, prior to graphing as relative absorbance and intensity, respectively.
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9

Characterization of NBP@TiO2 Nanostructures

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The transmission electron microscopy (TEM) images of the NBP@TiO2 nanostructures were captured on an FEI Tecnai Spirit microscope operated at 120 kV. High-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) characterization and elemental mapping were performed on an FEI Titan G2 60-300 microscope. The extinction spectra were measured on a Lambda 950 ultraviolet/visible/NIR spectrophotometer. The Au mass concentrations in the solution samples were measured on an Agilent 7500a inductively coupled plasma atomic emission spectrometry (ICP-AES) system. Fourier transform infrared spectroscopy (FTIR) analysis was performed on a Shimadzu IRAffinity-1S spectrophotometer. Thermogravimetric analysis (TGA) was carried out on a Perkin Elmer TGA 6 thermogravimetric analyzer, using a heating rate of 1 °C min−1. The hydrodynamic size of the CA4P-loaded NBP@TiO2 nanostructures was measured by a Malvern Zetasizer Nano ZS90 size analyzer.
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10

Comprehensive Characterization of N, S-Codoped Carbon Dots

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UV-visible absorption and fluorescence spectra were recorded using a UV-visible spectrophotometer (UV-2600, Shimadzu, Japan) and an LS55 luminescence spectrometer (Perkin-Elmer, USA), respectively. The elemental compositions of N, S-codoped CDs were obtained using an ESCALAB 250Xi X-ray photoelectron spectrometer (XPS, Thermo Electron, USA). Fourier transform infrared (FTIR) spectra were collected using the potassium bromide pellet methodology with an IRAffinity-1S spectrophotometer (Shimadzu, Japan). Transmission electron microscopy (TEM) and high-resolution TEM (HRTEM) images were obtained using a JEOL JEM-1200EX electron microscope operating at 120 kV with an accelerating voltage of 120 kV and an FEI Tecnai G2 F20 S-Twin electron microscope operating at 200 kV, respectively. The further determination of the concentration of Fe3+ in human serum was performed using an Agilent 7500ce inductively coupled plasma mass spectrometry (ICP-MS) system (Agilent Technologies, Japan).
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