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The IR 200 is a Fourier Transform Infrared (FTIR) spectrometer designed for general laboratory applications. It is capable of analyzing a wide range of organic and inorganic materials by detecting and identifying their molecular structures through infrared spectroscopy.

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2 protocols using ir 200

1

Characterization of Functional Nanocomposites

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The morphologies
and microstructures of functional nanocomposites were observed by
transmission electron microscopy (TEM, JEM-2010, JEOL, Japan) at an
accelerating voltage of 120 kV. Samples dispersed at an appropriate
concentration were dropped onto a carbon-coated Cu grid, followed
by air drying. The chemical structures and compositions of functional
nanocomposites were characterized by a Fourier transform infrared
(FT-IR) spectrometer (IR 200, Thermo Nicolet). The hydrodynamic sizes
of PNB were tested by a dynamic light scattering (DLS) instrument
(Zetasizer Nano-ZS, Malvern Instruments, UK) with a scattering angle
of 90°. Thermogravimetric analysis (TGA) of the functional nanocomposites
was performed on a Mettler TGA/SDTA851e° (Switzerland) at a heating
rate of 5 °C/min from 20 to 650 °C under a nitrogen atmosphere.
The magnetism of functional nanocomposites was measured by a vibrating
sample magnetometer on a model 6000 physical property measurement
system (Quantum Design). The stabilities of functional nanocomposites
during adsorption processes were measured using inductively coupled
plasma mass spectrometry (ICP-MS, Thermo Fisher).
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2

Characterization of Hydrogen Bonds and Thermal Properties

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The hydrogen bonds were characterized using a Fourier transform infrared (FT-IR) spectrometer (IR 200, Thermo Nicolet, USA). Polarized optical microscopy (POM) images were obtained using a Caikon microscope (XPF-500C) equipped with polarization filters. A CK-400 hot stage was used to conduct the thermo-controlled experiments. Differential scanning calorimetry (DSC) was performed using a TA instruments Q2000 calorimeter. The samples were heated or cooled at a rate of 10 °C min−1 with an isothermal equilibration of 2 min after each heating or cooling ramp. The thermogravimetric analyses (TGA) of samples were performed using a STA-449C (Germany). The samples were heated from 30 to 800 °C at a rate of 10 °C min−1 under a nitrogen atmosphere. The XRD patterns were collected on an Anton Paar Saxsess mc2 apparatus attached to an ID 3003 laboratory X-ray generator (General Electric) equipped with a sealed X-ray tube (PANalytical, λ (Cu-Kα) = 0.1542 nm, 40 kV, 50 mA). Adsorption kinetics were studied by UV-vis spectroscopy using a UV-vis spectrometer (Spectrum lab 752s, Shanghai). Other UV-vis spectroscopy experiments were performed using a UV-vis spectrophotometer (UV-1800PC, Mapada Instruments, Shanghai).
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