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102 protocols using nicolet is20

1

Thermal and Structural Analysis of PAM-LiCl&GFP Composites

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Fourier-transform infrared (FTIR) spectra of the samples were recorded by a Thermo Scientific Nicolet iS20 instrument (Waltham, MA, USA) at room temperature. The surface morphology and elemental distribution mapping of the samples were examined with a scanning electron microscope (SEM, Czech TESCAN MIRA LMS) and energy dispersive spectroscopy (EDS), respectively. Differential scanning calorimetry (DSC) was conducted using a TA Q2000, DSC2500 instrument (New Castle, DE, USA) to determine the thermal behavior of the PAM-LiCl&GFP. Measurements proceeded in a nitrogen atmosphere, with a heating pace of 5 °C∙min−1. Water sorption and desorption tests for the samples were performed in an MT/150 L chamber, maintaining constant temperature and humidity. This chamber allows adjustments in dry bulb temperature (DB) and RH as needed, with a consistent airflow at 2.15 m∙s−1 ensuring stable ambient conditions. The specific surface areas were calculated by the Brunauer–Emmett–Teller (BET) method via Micromeritics ASAP 2460 (Norcross, GA, USA).
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2

Characterization of Thermodegraded Polymer Powders

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The prepared pTDM and hTDM were placed in a low-temperature freezing-grinding instrument (JXFSTPRP-CL; Shanghai, China). The temperature was set to −50 °C, and grinding was performed at 60 Hz/min for 1 min. After repeating this step three to five times, the obtained powder was TDM powder. The chemical properties of the hTDM and pTDM powders were examined using Fourier-transform infrared (FTIR) spectroscopy (Thermo Scientific Nicolet iS20). Infrared spectra were recorded in the wavelength range of 400–4000 cm−1 using a beam splitter coated with Ge on a KBr detector with a resolution of 4 cm−1 (with 32 scans). Raman analyses of pTDM and hTDM powders were performed using DXR3 Flex Raman Spectrometer (Thermo Scientific DXR3) coupled with a Peltier-cooled Charge Coupled Device (CCD) detector. Excitation was provided by the 785 nm line of the diode laser. Spectra were collected from 100 to 3500 cm−1 wavenumber shifts at a spectral resolution of 2 cm−1 using a 60 s integration time.
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Comprehensive Characterization of Material Surfaces

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Scanning electron microscopy (SEM) images were taken by the scanning electron microscope (Hitachi S3700N, Japan). The contact angle data were obtained on a commercial contact angle system (JC2000C2, Powereach, China) at ambient temperature using a 5 mL droplet as the indicator. The material of the samples was analyzed by Fourier transform infrared spectrometer (FTIR) (Thermo Scientific Nicolet iS20, USA). X-ray photoelectron spectroscopy (XPS) measurements were performed by an AXISNOVA instrument (Thermo Fisher Scientific, K-ALPHA+, USA) using a monochromatic Al Kα X-ray source (1486.68 eV). Digital images and videos were captured using a CCD camera with 10M Micro Lens (Vitken, SHL-500 W-NEW, China) and high-speed camera (Phantom Mro311, USA).
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4

FTIR Analysis of Graphene Quantum Dots

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For FTIR analysis, powdered samples of GQD-EDA/1 g, GQD-EDA/5 g, and GQD-EDA/10 g, were mixed with KBr and compressed into pellets. Spectra were recorded using an FTIR spectrometer (Thermo Nicolet iS20, Waltham, Massachusetts, MA, USA) in the range of 4000–400 cm−1 at 32 scans per spectrum at 4 cm−1 resolution. For spectra analysis we used OMNIC 9 software version 9.9.509 by Thermo Fisher Scientific Inc. (Waltham, Massachusetts, MA, USA).
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5

Graphene Oxide-Microcystin-LR Composite Characterization

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5 mg of GO was weighed and added to 1 L of ultrapure water, and sonicated for 30 min to afford evenly dispersed GO suspension. MCLR solution (60 µL), in a concentration of 1 mg/mL, was added to prepared GO suspension, GO-MCLR composite solution was obtained after well mixing. A drop of GO/GO-MCLR solution was placed on the copper net and slowly dried with nitrogen, then morphologies of GO/GO-MCLR were observed and photographed by by spherical aberration corrected Transmission Electron Microscope (ACTEM) (FEI TITAN 80-300 operating at 80 kV). The hydration particle sizes of all samples were obtained by Malvern laser particle size analyzer (ZetasizerNano-ZS90, Malvern Instruments, UK). The surface chemical states and functional groups of GO and GO-MCLR were investigated by FTIR (Nicolet IS20, Thermo Fisher Technology LTD, China) and XPS (Shimadzu, Japan). Microscopical laser Raman spectroscopy (MLRM) (Renishaw inVia Reflex, Wotton under Edge, UK) was used to obtain atomic vibration, phonon scattering and other information to study the molecular structure of GO and GO-MCLR.
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6

Characterization of Flour Molecular Structure

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The presence of various functional groups was assessed by Thermo Scientific Nicolet iS20 (Massachusetts, USA) spectrometer equipped with an attenuated total reflectance ATR accessory. The FT-IR spectra of the WF and AF fractions were achieved at a spectral resolution of 4 cm−1 by 32 scans recorded between 650 and 4000 cm−1, the graphs being evaluated with OMNIC software (9.9.549 version, Thermo Fisher Scientific, Waltham, MA, USA) based on previous studies, in order to identify the molecular characteristics of the flours28 (link).
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7

Spectral Analysis of Lignin Samples

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A certain amount of culture solution was taken from the initial test liquid medium and the reacted E-F/P system, E-F system and P system and then dried under vacuum at 60 °C for 24 h. The obtained samples containing lignin were subjected to spectral scanning using the KBr press method with a Thermo Scientific Nicolet iS20 infrared spectrometer in the range of 400–4000 cm−1 with 32 scans and a resolution of 4 cm−1.
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8

Comprehensive Characterization of Lyophilized MB/BG@LG

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Scanning electron microscopy (SEM; Zeiss, Germany) was used to evaluate the appearance of the lyophilized system of MB/BG@LG. The elemental mapping of the materials was performed by combining scanning electron microscopy with energy dispersive spectroscopy (EDS; Inca Energy, England). Dynamic light scattering (DLS, Malvern Instruments, UK) was used to measure the bioglass diameter. Flight Test Instrumentation Requirements (FTIR; Thermo Scientific Nicolet iS20, USA) were performed to analyze the composition of MB/BG@LG. The morphology before and after release was observed by cryo-electron microscopy. (Cryo-SEM; Hitachi Regulus 8220; Japan).
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9

Characterization of Zwitterionic Hydrogel

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Fourier transform infrared spectra (FT-IR) analysis was used to examine the chemical structure of these samples. The freeze-dried hydrogels were ground into powder and pressed into disks by mixing with potassium bromide (KBr) powder. The spectra were measured with an FT-IR spectrophotometer (Thermo Scientific Nicolet iS20, Waltham, MA, USA) over the spectral range of 4000–400 cm−1.
To further prove the existence of the GO and β-TCP in the zwitterionic hydrogel, the characteristic phase and crystallinity were investigated via x-ray diffraction spectroscopy (Bruker D8 Advance) using 40 mA and 40 kV current. Data were recorded in the scanning range from 10° to 80° (2θ degrees) at a step size of 1°/min.
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10

Characterization of Titanium Dioxide Nanotubes

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The morphology and surface properties of the titanium dioxide nanotubes were observed using a field emission scanning electron microscope (SEM, ZEISS Gemini 300, Germany) and transmission electron microscope (TEM, JEM-1200EX, Japan). The crystalline structure of the TNTs and HNK-TNTs were analyzed by X-ray diffraction (XRD) (Bruker D2 Phaser). Fourier Infrared Spectroscopy (FTIR) (Thermo Scientific Nicolet iS20) was used to compare the composition of TNTs and HNK-TNTs.
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