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Nicolet is50 ft ir instrument

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Nicolet iS50 FT-IR instrument is a Fourier Transform Infrared spectrometer designed for analytical applications. It utilizes infrared light to identify and quantify chemical compounds in a sample. The instrument records the absorption or transmission of infrared radiation by the sample, and the resulting spectrum can be used to determine the molecular structure and composition of the analyzed material.

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12 protocols using nicolet is50 ft ir instrument

1

Characterizing PU Polymer Structure

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The molecular structure of PU polymers was evaluated with Attenuated Total Reflection Fourier Transform Infrared spectroscopy (ATR‐FTIR) using a Nicolet iS50 FT‐IR instrument (Thermo Scientific). All spectra were collected with 32 scans and at a resolution of 4 cm−1. The raw data was analyzed with the software OMNICTM provided with the instrument.
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2

Characterization of GlcNAc-Functionalized Silica Sorbent

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All HPLC separations were performed using Waters Alliance 2629 separation module (Milford, MA, USA), connected with an in-line degasser, a quaternary solvent pump, an autosampler, and a thermostated column compartment. A Waters PDA detector (model 2475) was used to record the signals at 254 nm. All the chromatographic separations were carried out by maintaining the column at room temperature. N-Acetylglucosamine functionalized-silica (GlcNAc-silica) slurry was packed in stainless-steel columns using a constant pressure pump from Shandon Southern Products Ltd. (Rincon, Cheshire, UK). Data acquisition was performed using Empower 2 (Build 2154) software (Waters Chromatography), and then the offline chromatographic data were processed using OriginPro v8.5.1 (Origin Lab Corp., Northhampton, MA, USA). Fourier transform infrared (FTIR) analyses were carried out for the characterization of GlcNAc-silica sorbent using attenuated total reflectance mode on a Nicolet IS50 FT-IR instrument from Thermo Scientific Co. (Waltham, MA, USA). Furthermore, the functionalization of silica with surface bound N-acetylglucosamine was assessed via thermogravimetric analysis using a Q-50 thermogravimetric analyzer from TA instruments (New Castle, DE, USA). Approximately 8–10 mg of the samples was heated from 20 °C to 900 °C at a heating rate of 20 °C per min with a 40 mL/min continuous nitrogen gas flow.
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3

Comprehensive Characterization of MBCDs

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The surface morphology of the MBCDs was examined by transmission electron microscopy (TEM, FEI Tecnai 30) and Atomic Force Microscope (AFM, Dimension Fastscan. The phase composition of the MBCDs was characterized by X-ray diffraction (Rigaku D/max 2550 VB + 18 kW with Cu Kα′ radiation) and X-ray photoelectron spectroscopy (PHI Quantera XPS). The Fourier transform infrared (FTIR) spectra of the MBCDs was collected by the Thermo Nicolet iS50 FT-IR instrument (Thermo Scientific, USA). The fluorescence properties were determined by fluorimeter (FluoroMax-4, HORIBA Jobin Yvon, France).
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4

Comprehensive Nanomaterial Characterization

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FTIR spectrum was recorded on Nicolet iS50 FT-IR instrument from Thermo Scientific. Morphology of the synthesized NPs was visualized through transmission electron microscopy (TEM) and Field emission scanning microscopy (FE-SEM) on Hitachi H-7500 and Hitachi-SU8010 microscope respectively. Elemental analysis of the product was resolute from EDS coupled with FESEM instrument. Images of the dried pattern were captured using Carl ZEISS Axio Imager.2Am microscope. Captured images were analyzed by axio-vision software.
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5

Characterization of Wood-Based Materials

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The wood, cellulose network, and CPP samples were characterized with a scanning electron microscope (SEM) using a Hitachi S-3400N SEM (Tokyo, Japan) with an acceleration voltage of 5 kV. The Fourier transform infrared (FTIR) spectra of the wood, cellulose network, PANI, and CPP samples were measured with a Nicolet iS 50 FTIR instrument (Thermo Fisher Scientific Corp., Waltham, MA, USA). The spectra of each sample were recorded from 400 to 4000 cm−1 with 32 scans at a resolution of 4 cm−1. The ultraviolet–visible (UV−vis) spectra of electrode materials and devices were measured via a PerkinElmer Lambda 950 UV−vis spectroscopy (Waltham, MA, USA) with the wavelength of 250–800 nm. A three-electrode system was employed to investigate the electrochemical properties of the samples electrodes in 1 M H2SO4 electrolyte at room temperature. A silver-silver chloride (Ag/AgCl) electrode and Pt electrode were used as the reference and counter electrodes, respectively. The electrochemical properties of electrodes were tested by cyclic voltammetry (CV), galvanostatic charge–discharge (GCD) and electrochemical impedance spectroscopy (EIS) measurements on a Corrtest CS 310H electrochemical workstation (Wuhan, China).
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6

Multimodal Characterization of Filaments

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Chemical characterization of the filaments was accomplished with Fourier transform infrared spectroscopy (FTIR), NMR, and laser-induced breakdown spectroscopy (LIBS). Absorption spectra were obtained in attenuated total reflectance (ATR) mode using a Nicolet iS50 FTIR instrument (Thermo Fisher Scientific, Waltham, MA, USA) equipped with a diamond crystal reference. Scans measured the absorbance from 525 to 4000 cm−1 at a resolution of 4 cm−1, and spectra reported here are background-subtracted and averaged from 32 scans per sample. For NMR, samples were dissolved in deuterated chloroform over 48 h, and the resulting solutions were extracted with filtered syringes and placed in NMR tubes. Extracts were analyzed via liquid-state 1H NMR experiments using a Bruker Avance NMR spectrometer (Bruker Corporation, Billerica, MA, USA) operating at 500.13 MHz, and residual protons in the solvent were used as a proton reference. Elemental makeup and distribution of the filaments were determined via a LIBS-based elemental analyzer (Keyence EA-300 VHX Series; Keyence Corporation, Osaka, Japan) attached to a Keyence VHX-7000 microscope. The spot size for LIBS analyses was 10 µm and element concentrations were averaged from three analyses per spot.
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7

FTIR Analysis of Dried Samples

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FTIR analysis was performed using a Thermo Scientific, Nicolet iS50 FTIR instrument (Massachusetts, USA) in attenuated total reflectance mode with a diamond plate and ZnSe lens. The samples were dried at 90 °C on a hot plate before analysis.
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8

Synthesis and Characterization of LE Conjugate

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The LE conjugate used in this study was synthesized according to the methods of Lei et al. [30 ]. Briefly, 100 mL of CS solution (0.5%, m/V) in a 150 mL glass flask was adjusted to pH 3.5 with NaOH (10 M), followed by the addition of 1 mL of H2O2 (0.5 M) containing ascorbic acid (0.025 g). After stirring for 1 h, EGCG was added, and the solution was allowed to react for 12 h with magnetic stirring at 40 °C. The resulting solution was dialyzed (molecular weight cut-off: 14,000 Da; Millipore, Billerica, MA, USA) for 72 h and then lyophilized to obtain the LE conjugate. The 1H nuclear magnetic resonance (1H NMR) spectrum of LE was recorded on a Bruker Avance III 400 M instrument (Bruker, Frankfurt, German) at 400 MHz using D2O as the solvent. Fourier transform infrared (FTIR) spectra and ultraviolet visible (UV-vis) absorption spectra of LC, EGCG, and LE were obtained with a Nicolet™ iS50 FTIR instrument (Thermo Fisher Scientific Inc., Waltham, MA, USA) and a UV-vis spectrophotometer (UV-2550; Shimadzu, Kyoto, Japan), respectively.
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9

Characterization of Au-prGO Nanocomposites

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Transmission electron microscopy (TEM). The Au-prGO nanocomposites were visualized using TEM (JEOL JEM-1230 TEM). A small volume of the processed solution was dropcasted onto a carbon-coated grid (Ted Pella, Inc.) and left to dry for at least 24 hours. Size distributions of the Au NPs were measured using ImageJ software from different areas of the TEM grid.
Fourier transform infrared spectroscopy (FTIR). FTIR measurements were obtained using the Thermo Scientific, NICOLET iS50 FT-IR instrument. The Diamond Attenuated Total Reflectance (DATR) attachment was used along with the KBR beamsplitter and the DTGS detector.
Raman spectroscopy. Raman spectra were obtained using the Thermo Scientific DXR SmartRaman instrument at 532 nm and 10 mW. An aperture slit of 25 mm was used along with a 180 degree accessory.
X-ray diffraction (XRD). A PANalytical MPD X'/Pert Pro diffractometer with voltage 45 kV and current 40 mA was used to measure the X-ray diffraction patterns at room temperature using Ni-filtered Cu Ka 1 radiation.
X-ray photoelectron spectroscopy (XPS). Spectra were obtained using the ThermoFisher Scientific ESCALAB 250 with a microfocused monochromatic AlKa X-ray source (15 kV) and a doublefocusing full 1801 spherical sector electron analyzer.
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10

Freeze-dried Colloidal Particle FTIR Analysis

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The SPI-SA colloidal particle suspension was freeze-dried. The dried colloidal particle powders were then mixed with potassium bromide. FTIR of the colloidal particles with a wavenumber range of 4000–400 cm−1 was measured with a Nicolet iS50 FTIR instrument (Thermo Fisher Scientific, China) (Gao et al., 2023 ).
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