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60 protocols using nicolet 8700

1

FTIR Analysis of Waterborne Polyurethane Films

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The FTIR spectra of dry films from WPU emulsion samples were performed between 4000 and 500 cm−1 on a Nicolet 8700 Fourier transformed infrared spectroscopy (FTIR, Thermo Nicolet Corporation).
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2

Comprehensive Characterization of WSe2-PVP NPs

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The surface morphology was analyzed via a TEM (H‐700, Hitachi, Ltd., Tokyo, Japan). Meanwhile, energy dispersive spectrometer was performed to measure surface elements of WSe2‐PVP NPs. Chemical state analysis of samples was characterized using XRD (X'Pert Pro, Netherlands). The chemical bonds and functional groups of synthetic WSe2‐PVP NPs were characterized using FT‐IR spectral (Nicolet 8700, Thermo Nicolet, Madison, USA) and Raman spectra (Jobin‐Yvon, Horiba Group, France). The XPS measurement equipment was conducted to analyze the chemical composition of the synthetic WSe2‐PVP NPs.
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3

Kinetic Analysis of Thiol-Ene-Azide Reactions

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The kinetics (presented in the Supporting Information) were analyzed using a Fourier transform infrared spectrometer (Nicolet 8700, Fisher Scientific) in transmission mode, combined with a heating stage set at 60 °C. Irradiation of samples placed between NaCl plates was performed using a light guide connected to a mercury lamp (Acticure 4000, EXFO) with a 365 nm bandgap filter and an irradiance of 10 mW cm−2. The thiol, ene, and azide peaks of the monomers were monitored in the absorption range between 2602 and 2525 cm−1, 956 and 920 cm−1, and 2250 and 2000 cm−1, respectively, with 4 scans s−1 and at 2 cm−1 resolution.
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4

Real-Time Polymerization Kinetics Monitoring

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An FTIR spectrometer (Nicolet 8700, Fisher Scientific) incorporated with a heating stage was used to monitor the real-time polymerization kinetics of the functional group conversion in transmission mode. Irradiation was performed using a light guide connected to a mercury lamp (Acticure 4000, EXFO) with either a 365 nm or 400–500 nm bandgap filter, depending on the photoinitiator used. Samples were placed between NaCl plates, and the azide peak was monitored in the absorption range between 2300–2000 cm−1 having the alkane C–H stretching bonds as a reference peak between 2980–2840 cm−1 with 12 scans s−1 and 2 cm−1 resolution.
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5

FT-IR Spectroscopic Characterization of Microbial Strains

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The FT-IR spectra were measured using the FT-IR spectrometer (Nicolet 8700; Thermo Electron Corp., Waltham, MA, USA) equipped with the GoldenGate (Specac Corp., Orpington, UK) ATR accessory with a single reflection diamond crystal. The temperature of the crystal was maintained at 25.0 ± 0.1 °C by using an automatic temperature controller (Specac Corp, Orpington, UK) coupled with the ATR accessory. In each measurement, 64 scans were collected with a resolution of 4 cm−1 and the range of 4000–550 cm−1. The spectrum of the filament was measured and later subtracted from every measured spectrum as the background. After measuring all FT-IR spectra corresponding to a selected strain and background subtraction, the average spectrum was calculated. The spectrometer was purged with dry nitrogen to diminish the negative influence of water vapor. Spectragryph V1.2.10 software (Oberstdorf, Germany) was used to process the obtained spectra.
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6

Biodegradation Impact on PE Structure

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PE polymeric structural change after biodegradation under a high methane dose was recorded by Fourier-transform infrared spectroscopy coupled with attenuated total reflectance (FTIR–ATR; Nicolet 8700, Thermo Electron Co., Waltham, MA, USA) with a scanning power with a resolution of 4 cm−1 and a 500–4000 cm−1 range. PE samples from all treatments including the control (non-inoculated sample) were subjected to FTIR analysis.
PE biodegradation was further confirmed through gel permeation chromatography (GPC) by evaluating the molecular weight changes. A PL-GPC PL50 (Agilent, Santa Clara, CA, USA) system coupled with the triple mixed-b columns and an RI detector was used for this purpose.
PE was solubilized in 1,2,4-tricholobenzene (TCB) and 0.15 butylated hydroxytoluene (BHT) at 160 °C and the same chemicals were used as eluents in GPC. The eluent flow rate was maintained at 1 mL min−1 with a column temperature of 160 °C. Agilent chemstation software A.10.02 (Agilent, Santa Clara, CA, USA) was used for data analysis and Agilent (Agilent, USA) polystyrene standards were used for calibration curves.
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7

Characterization of Polymer Crosslink Density

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A WD-4005 AGS-J electronic universal testing machine (Shimadzu Corporation, GB/T 528-1998) was used to perform tensile tests using dumbbell-shaped samples at 25 °C with a strain rate of 100 mm min−1. The crosslink density was examined with a VTMR20010V-T low-field NMR spectrometer provided by the Shanghai Newman Corporation. Fourier-transform infrared spectroscopy (FTIR) measurements were performed using a Nicolet 8700 from the Thermo Electron Corporation. These were performed with 48 scans in the middle infrared region with a spectral resolution of 2 cm−1 and spectral range 4000–500 cm−1. Binder samples with masses of 10 mg were placed in alumina pans and subjected to differential scanning calorimetry (DSC) analysis in a Setaram DSC131 under a nitrogen atmosphere at a flow rate of 40 mL min−1 with a heating temperature range of −100 to 150 °C.
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8

FT-IR Spectral Analysis of Bacterial Strains

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The FT-IR spectra were measured using a spectrometer (Nicolet 8700; Thermo Electron Corp., Waltham, MA, USA) equipped with the GoldenGate (Specac Corp., Oprington, UK) ATR accessory with a single reflection diamond crystal. The temperature of the crystal was maintained at 25.0 ± 0.1 °C by using an automatic temperature controller (Specac Corp., Orpington, GB) coupled with the ATR accessory. In each measurement, 64 scans were collected with a resolution of 4 cm−1 and the range of 4000 to 550 cm−1. The spectrum of the filament was measured and later subtracted from every measured spectrum as the background. After measuring all FT-IR spectra corresponding to a selected strain and background subtraction, the average spectrum was calculated. The spectrometer was purged with dry nitrogen to diminish the negative influence of water vapor. Spectragryph V. 1.2.10 software (Oberstdorf, Germany) was used to process the obtained spectra.
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9

FTIR Spectroscopic Analysis of Samples

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A Fourier-transform infrared (FTIR) spectrometer (Nicolet 8700, Thermo Electron Corp, Madison, WI, USA) equipped with a Nicolet Smart Orbit attenuated total reflectance (ATR) accessory and diamond internal reflection element was used to analyze the samples. The spectra were recorded in the wavenumber range of 4000-500 cm -1 at a resolution of 4 cm -1 by 64 scans. For each scanning, the spectrum was collected by subtracting the origin spectrum by the air background spectrum.
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10

FTIR Analysis of Modified AX Films

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Fourier-transform infrared (FTIR) spectroscopy was used to determine the interaction in structures between modified and unmodified AX films [45 (link)]. The testing condition was at 4 Reciprocal Centimeter (cm−1) resolution and 10 Aperture, with the range of the wavenumber between 4000 and 700 cm−1 (Thermo Scientific, Nicolet 8700, Wilmington, DE, USA).
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