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35 protocols using nicolet is5 ftir

1

FTIR-ATR Analysis of Zirconia Tablets

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A Nicolet iS5 FTIR (Thermo Scientific; Waltham, MA, USA) infrared light source was directed at a fixed mirror and a moving mirror to be combined into a single infrared light. Fourier transform infrared spectroscopy – attenuated total reflectance (FTIR–ATR) provides information related to the presence or absence of specific functional groups, as well as the chemical structure of polymer materials. Since zirconia tablets are opaque, we use semi-attenuated total reflection (ATR) for measurement.
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2

FT-IR Analysis of Crude Polysaccharides

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FT-IR spectra of crude polysaccharides were recorded on a Fourier-transform infrared spectrometer (Nicolet iS5 FT-IR, Thermo Fisher Corporation, USA) in the range of 400–4000 cm−1 at room temperature. Each polysaccharide was incorporated with KBr powder at a ratio of 1: 100, pressed into a pellet, and then scanned for FT-IR measurement.
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3

Characterizing Soil Carbon Composition via ATR-FTIR

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Attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) was used to determine C compositions in residue and heavy soil fractions. The spectra data were acquired at the resolution of 4 cm−1 after 100 scans across a range of 4000 to 400 cm−1 using a Thermo Scientific Nicolet iS5 FTIR. Ambient air was used as background for all samples. The spectra were converted to absorbance (log 1/R), smoothed, corrected for baseline and then averaged (n = 3) for each treatment. Data collection and spectral calculations were accomplished using OMNIC software version 8.2.0. All spectra were analyzed at the below-mentioned absorption bands to indicate specific functional groups. Specifically, the absorption bands at 2950–2860 cm−1 were assigned to aliphatic C-H band41 (link). The bands at 1738, 1722 and 1712 cm−1 were assigned to C=O stretching in lactones, ketones, aldehydes, and fatty acids42 (link). The bands at 1600–1640 cm−1 were assigned to C=O groups in amides and carboxylic acids or aromatic C=C groups43 (link). The bands at 1547, 1529 and 1514 cm−1 were assigned to C=C groups of aromatic compounds and N–H groups of amides42 (link).
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4

ATR-FTIR Spectra of Protein Samples

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ATR-FTIR spectra were measured with a Nicolet iS5 FT-IR equipped with an iD5 ATR accessory (Thermo Fisher Scientific, Waltham, MA, USA). Samples of all pH conditions were precipitated by centrifugation in the presence of 0.5 M NaCl and resuspended in water. This process was repeated three times to replace the buffer solution in the sample with water. The suspension was placed on a diamond crystal prism and then dried. FTIR measurement was performed by collecting 128 interferograms at a resolution of 4 cm−1.
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5

Comprehensive Analytical Characterization

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Reagents were used as received from Sigma-Aldrich,
Fischer Industries, Acros Organics, Alfa Aesar, and Merck Schuchardt.
NMR spectroscopy was carried out at 400 MHz using Bruker AV400 and
Bruker AV(III)400 spectrometers. IR spectroscopy was carried out using
a Bruker Tensor 27 FTIR or Thermoscientific Nicolet iS5 FTIR with
an iD5 ATR attachment. ESI mass spectrometry was undertaken using
a Bruker Daltonics microTOF electrospray mass spectrometer and MALDI
mass spectrometry using a Bruker Ultraflex III spectrometer equipped
with a matrix-assisted laser desorption ionization source and used
a DTCB matrix. Elemental analysis was undertaken using an Exeter Analytical
CE-440 Elemental Analyzer.
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6

Infrared Spectroscopy Analysis of Pressed Samples

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AP, GMS, blank NLC, and AP-NLC were respectively crushed with potassium bromide crystals, fully mixed, and then pressed into transparent sheets. The infrared absorption spectrum was analyzed by Nicolet iS5 FT-IR (Thermo Fisher Scientific, Waltham, MA, USA). The wave number scanning range was set to 400–4000 cm−1.
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7

Spectroscopic and Thermal Characterization of Materials

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1H nuclear
magnetic resonance (1H NMR) spectra were recorded on a
JEOL JNM-ECX400 spectrometer at resonant frequencies of 400 MHz in
deuterated dimethyl sulfoxide (DMSO-d6) at 50 °C, DMF-d7 at room temperature,
or on a JEOL JNM-ECZ600/ M1 spectrometer at resonant frequencies of
600 MHz in DMF-d7 at 90 °C. 13C NMR was recorded on a JEOL JNM-ECZ600/M1 spectrometer at
resonant frequencies of 150 MHz in DMF-d7 at 90 °C. The logarithmic viscosity method was employed to
measure the viscosity using an Ostwald viscometer and a thermostatic
bath (TV-5S, Thomas Kagaku Co., Ltd.). The samples were dissolved
in concentrated H2SO4 and adjusted to 0.5 dL/g,
and the flow time was measured at 30 °C. FTIR spectra were measured
using a Thermo Fisher Scientific Nicolet iS5 FTIR with the sample
ground. TG/DTA 6300 and DSC 6200 were used for thermal characterization.
TGA was performed by placing an aluminum pan containing a sample (<10
mg) on a balance in a weighing chamber. The heating rate was set to
10 °C/min; the scan started at room temperature and ended at
550 °C, followed by holding for 10 min. For DSC measurements,
the maximum temperature was set at approximately 20 °C below
the 1% weight loss temperature obtained by TGA of the same sample.
The heating and cooling rates were set to 10 °C/min, and the
1st cooling scan and 2nd heating scan were taken to determine the Tc and Tg/Tm values, respectively.
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8

Xanthan Analysis by FTIR Spectroscopy

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Fourier transform infrared spectroscopy (Nicolet iS5 FTIR ThermoFisher) was used to analyze digested xanthan. The test mode was set to through, and the resolution of the mid-infrared zone and the near-infrared resolution were set to better than 0.4 cm−1 and 0.1–6.4 nm, respectively. The spectral range was 15,000–450 cm−1, and the signal-to-noise ratio was set to lower than 250,000:1. The scanning speed was 0.1–4.0 cm/s, and the wavenumber accuracy was set to better than 0.008 cm−1.
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9

Structural Analysis of Modified Silk

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The structural conformations of modified silks (either as lyophilized powders or films) were analyzed with a Nicolet iS5 FT-IR equipped with an iD7 diamond attenuated total reflectance (ATR) accessory (Thermo Scientific, Waltham, MA). The absorbance of samples was measured between 4000 – 400 cm−1, with 64 scans, and a resolution of 4 cm−1. Background spectra were collected under the same conditions and subtracted from the sample. All samples were analyzed after 24 hours with or without methanol (100% v/v) treatment.
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10

Characterization of Graphene Quantum Dots

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The size and morphology of GQDs was analyzed by using a JEM 2100F transmission electron microscope at an operating voltage of 200 KV. The height distribution of the GQDs was characterized by atomic force microscope (AFM) (Bruker Multimode, Bruker Corporation, Billerica, MA, USA) operating in tapping mode. The X-ray diffraction (XRD) pattern was measured using a Bruker-D8 Advance (Bruker Corporation) and Cu Kα radiation (λ=1.54051 Å) operating at 1 KV. The Fourier transform infrared spectroscopy (FTIR) spectra were measured by a Nicolet iS5 FT-IR (Thermo Nicolet, Thermo Fisher Scientific) spectrometer with the KBr pellet technique. X-ray photoelectron spectroscopy (XPS) was performed using a Thermo Scientific Escalab 250Xi with Al Kα X-ray radiation as the X-ray source for excitation. Binding energies were corrected using the C1s peak at 284.6 eV as the standard. PL spectra of GQDs were recorded using a Cary Eclipse fluorescence spectrophotometer (Agilent Technologies, Santa Clara, CA, USA). The fluorescence lifetime was measured using a photo-counting HORIBA FL-4 system, with a diode laser emitting at 330 nm as the light source.
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