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23 protocols using cary 660 ftir spectrometer

1

Comprehensive Characterization of Colloidal Nanoparticles

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Transmission electron microscopy (TEM) (JEOL Ltd, Japan) was used to analyze the morphology of CDs. A Nano ZS/ZEN3690 (Malvern, UK) was employed to investigate the particle size distribution. The Fourier transform infrared spectroscopy (FT-IR) spectra were recorded from a Cary 660 FT-IR Spectrometer (Agilent, USA). The UV absorption spectra and the fluorescent spectra were respectively recorded using a U-3900 spectrophotometer (Hitachi, Japan) and the fluorescence spectrophotometer F-4600 (Hitachi, Japan). A Kratos AXIS Ultra DLD X-ray Photoelectron Spectrometer (Shimadzu, Japan) was used to analyze the surface characterization.
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2

ATR-SEIRAS Characterization of Bimetallic Catalysts

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A two compartment polytetrafluoroethylene cell with three electrodes was used for ATR-SEIRAS measurements. The schematic of the cell and steps to prepare chemically deposited gold film on the silicon ATR crystals can be found in our previous study (35 (link)). The working electrode was the bimetallic catalyst drop casted on the gold film on the silicon ATR crystals with catalyst loading of 0.4 to 0.5 mg cm−2. The catalyst inks were prepared by dissolving 5 mg of catalyst in 1 μl of Nafion solution (5 wt % in 50/50 water and isopropanol) and 250 μl of isopropanol. A graphite counter electrode was placed in one compartment, and a working electrode and Ag/AgCl reference electrode (3.0 M NaCl, BASi) were placed in the other compartment with gas inlet and purge lines. Two compartments were separated by a Nafion ion exchange membrane (Nafion 211, Fuel Cell Store). Potassium hydroxide solution (0.1 M; Sigma-Aldrich; 99.99%) was used as the electrolyte. The electrodes were connected to a potentiostat (Solartron 1260/1287) to apply potentials during measurements. The cell is integrated into the Agilent Technologies Cary 660 FTIR spectrometer equipped with a liquid nitrogen–cooled mercury-cadmium-telluride detector. All spectra were collected with 64 coadded scans and 4 cm−1 resolutions.
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3

Collagen Purification and FTIR Analysis

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Type I collagen was used as an analog of dentin collagen fibril, which was treated with HEMA immersion and plasma treatment. In order to fully remove physically adsorbed HEMA on collagen, acetone was used to thoroughly wash collagen immersed with HEMA. Acetone was selected because it is a good solvent for HEMA but not for collagen, which cannot be dissolved by acetone. After washing thoroughly with acetone, the collagen was dried in vacuum. FT-IR spectra were obtained by KBr pellets technique which were taken on a Cary 660 FT-IR spectrometer (Agilent Technologies, USA) in the absorption mode and averaged from 32 scans.
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4

Synthesis of Perovskite and Oxide Catalysts

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LaFeO3 (lanthanum
ferrate), Fe2O3 (ferrous oxide), and ZrO2 (zirconium oxide) were synthesized
by the solution combustion method using stoichiometric amounts of
lanthanum nitrate, ferrous nitrate, and zirconyl nitrate as precursors,
respectively, and glycine as the fuel. Combustion synthesis of LaFeO3, Fe2O3, and ZrO2 was carried
out at 300 °C according to standard procedures.34 (link) All of the catalysts were calcined at 600 °C in air
ambience for 3 h prior to use in experiments. Powder X-ray diffraction
(XRD) profiles of the catalysts were recorded in a D8 Discover (Bruker)
diffractometer using Cu Kα radiation at a scan rate of 8°
min–1. The pore size distribution
of the catalysts was obtained using a Micromeritics ASAP 2020 porosimeter.
Nitrogen adsorption–desorption isotherms were collected at
77 K, and specific surface area and pore size distribution were determined
using Brunauer–Emmett–Teller and Barrett–Joyner–Halenda
methods, respectively. FTIR spectra of the catalysts were obtained
using an Agilent Cary 660 FTIR spectrometer in the wavenumber range
of 700–4000 cm–1 in the attenuated transmittance
and reflectance mode at a resolution of 2 cm–1.
The surface morphologies of the catalysts were characterized using
a high-resolution scanning electron microscope (Hitachi S-4800 SEM).
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5

Infrared Spectroscopy of GTX-NLC Formulations

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The infrared spectra of the samples were collected using an Agilent Cary 660 FTIR Spectrometer (650–4000 cm−1). The bench consisted of a MIRacle Attenuated Total Reflection (Pike Technologies) fitted with a single-bounce, diamond-coated ZnSe internal reflection element. Samples of pure GTX, pure lipid excipients, their corresponding physical mixture, placebo formulation, and the lead GTX-NLC were analyzed.
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6

FTIR Spectroscopic Characterization of ARP-ADP Cocrystals

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FTIR spectra of pure ARP, ADP, and ARP-ADP cocrystals were obtained with a Cary 660 FTIR Spectrometer (Agilent Technologies, Santa Clara, California, USA) equipped with a MIRacle ATR (Pike Technologies, Madison, Wisconsin, USA) fitted with a single-bounce, diamond-coated ZnSe internal reflection element. A small sample was placed on the crystal surface and pressed using the built-in pressure tower to obtain uniform solid–crystal contact. The spectra were recorded in absorbance mode in the range of 600 to 4000 cm−1 with 16 scans and 4 cm−1 resolutions. An infrared microscope (Agilent Technologies, Santa Clara, California, USA) equipped with a 64 × 64 focal plane array detector and germanium micro ATR sampling accessory was used to collect the chemical images. Images were recorded at a field of view of approximately 70 × 70 µm and a spatial resolution of 1.1 µm.
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7

In situ SEIRAS study of CO electrooxidation

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In situ SEIRAS tests were conducted in a home-designed spectro-electrochemical cell with a three-electrode configuration as shown in Fig. 1a. The obtained metal film deposited on Si ATR crystal was used as the working electrode, a graphite rod as the counter electrode, and a saturated Ag/AgCl (BASI) as the reference electrode. The graphite rod was used as the counter electrode in order to avoid any metal contamination83 . During the test, CO gas was kept bubbling into the electrolyte and the system was mechanically stirred. The potential on the cell was supplied by a Solartron 1260/1287 system for electrochemical measurements. SEIRA spectra were collected by an Agilent Technologies Cary 660 FTIR spectrometer equipped with a liquid nitrogen-cooled MCT detector. All spectra were collected at a 4 cm−1 spectral resolution and presented in absorbance units where a positive and negative peak signifies an increase and decrease in the interfacial species, respectively. All SEIRA spectra presented in this work correspond to 64 coadded scans lasting about 40 s. After the SEIRAS experiment, the working electrode was removed from the SEIRAS cell, rinsed with DI water, and dried with blowing air.
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8

FTIR Structural Elucidation of PUEt Scaffolds

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Structural elucidation of the chemical composition of PUEt scaffold matrices was carried out using a Cary 660 FTIR spectrometer from Agilent Technologies equipped with a Germanium crystal ATR accessory. The FTIR spectra of the sample were taken in the MIR range (400–4000 cm-1) with a resolution of 2 cm-1.
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9

FTIR Analysis of Sample Functional Groups

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Fourier transform infrared (FTIR) spectra of the samples were recorded using a Cary 660 FTIR spectrometer with ATR assembly from Agilent Technologies, Santa Clara, CA, USA. Spectra were collected at 4 cm−1 resolution, with 256 scans per sample, in the range of 600–4000 cm−1. The purpose of the analysis was to identify the functional groups present in the samples.
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10

FTIR Analysis of ARP and Coformers

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FTIR spectra of ARP, the coformers and the ARP-SA and ARP-NA systems were recorded on a Cary 660 FTIR spectrometer (Agilent Technologies, Santa Clara, California, USA) to determine the intermolecular interactions. A small amount of powder sample was placed on the diamond crystal surface and pressed using the attached arm to provide uniform solid-crystal contact. The spectra were collected in the scanning range of 600-4000 cm−1 with a data resolution of 4 cm−1 and 16 scans.
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