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78 protocols using tg 209 f1 libra

1

Thermogravimetric Analysis of Samples

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Thermogravimetric (TG) analysis of the samples was carried out on the Netzsch TG 209 F1 Libra thermobalance in an oxidative atmosphere (temperature range 30–950°C, heating rate 10°C/min).
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2

Thermal Characterization of LDPE/MC Composites

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Differential scanning calorimetry (DSC; Q10 TA instrument, New Castle, DE, USA) was used to determine the thermal characteristics of LDPE/MC composite films at a heating rate of 10 °C/min under a nitrogen atmosphere. The thermal stability of an LDPE/MC composite was investigated using thermal gravimetric analysis (TGA; TG 209 F1 Libra®, NETZSCH, Selb, Germany). Samples weighing 10 mg were scanned at temperatures ranging from 30 to 700 °C under a nitrogen atmosphere at a rate of 20 °C/min. Values of onset degradation temperature and peak temperature were analyzed from TGA curves.
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3

Thermogravimetric Analysis of Samples

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TG 209
F1 Libra (NETZSCH) with an automatic sample feeder was used to perform
thermogravimetric analysis (TGA). The samples (10–15 mg) were
weighed into Al2O3 crucibles and analyzed over
a temperature range from 25 to 800 °C with a temperature increment
of 5 °C/min. The test was conducted under a nitrogen atmosphere
with the gas flow rate fixed at 50 mL/min.
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4

Synthesis and Characterization of Crosslinked Polymers

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EXAMPLE 1

Materials and Methods:

Phenol (Ph), ethylene glycol (EG), diethylene glycol (DEG), triethylene glycol (TEG) and Tetraethylene glycol (TETA) and paraformaldehyde were purchased from Fluka Chemie AG (Buchs, Switzerland). heptane was supplied by Sigma-Aldrich, Germany. All other solvents and reagents employed were of analytical grade. The infrared spectra were recorded were analysed by Perkin Elmer 16F PC FTIR spectrometer in the 4000-500 cm-1 wavelength region. The solid NMR spectra were recorded by Bruker WB-400 spectrometer with a spinning rate of 10 KHz. The cross-linked polymers were analysed for powder xray diffraction by Rigaku Miniflex II Desktop X-ray Diffractometer with 30 and stop angle of 700 sampling step size of 0.03, scan speed 3.00, 30 KV and 15 mA. The concentrations of mercury samples before and after analysis were analysed Inductively Coupled Plasma Mass Spectroscopy model ICP-MS XSeries-II (Thermo Scientific). Thermal properties of the synthesized cross-linked polymers were performed on NETZSCH Thermal Analyzer, model DSC 204 F1 Phoenix and TG 209 F1 Libra, respectively.

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5

Thermal and Spectroscopic Analysis of Calcined Phosphorite

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A TG analyzer (model: TG 209 F1 Libra) produced by NETZSCH GmbH (Selb, Germany) and FITR (model: iS50) of Thermo Fisher Scientific (Waltham, MA, USA) were used to perform thermal analysis and measure the TG characteristics and infrared (IR) curve of the samples. The test parameters were as follows: 20 mg of a sample in a nitrogen atmosphere was heated from 35 °C to 1100 °C, with heating rates of 10, 20, 30, and 40 °C min−1; the sampling parameter resolution of the Fourier Transform Infrared Spectrometer was 4 cm−1; and the wavenumber range was 4000–400 cm−1. An X-ray diffractometer (model: Panaco Empyrean) was used to analyze the phase composition of calcined phosphorite. The test conditions were: voltage of 40 kV, current of 40 mA, continuous scanning, scanning range of 10–80°, and scanning speed of 2° min−1. The chemical composition of the calcined phosphate tailings was analyzed using an X-ray fluorescence (XRF) analyzer. A TG analyzer and MS (PE TGA8000-FRONTIER-SQ8) were used to detect the distribution of volatile matter and gases with reaction temperature from the pyrolysis. The detection conditions were: He gas 99.999% atmosphere and a carrier gas flow rate of 20 mL min−1.
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6

Thermal-Spectroscopic Analysis of Ionic Liquids

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A TG 209 F1 Libra from Netzsch was coupled via transfer line with a Fourier Transform Infrared Spectrometer (FTIR) Vertrex 80v from BRUKER. The measurement was carried out in an argon atmosphere with a gas flow of 75 mL⋅min−1 in a temperature range from 40 °C to 300 °C at a heating rate of 1 K⋅min−1. Platinum crucibles without lids were used and a sample quantity of 26±2 mg for [C4C1im]BF4 and 6±1 mg for SeO2 was weighed in. The head temperature of the TGA was 200 °C and the transfer line was tempered to 230 °C to prevent condensation of the gaseous species formed. The gas cell of the FTIR was heated to 200 °C. Spectra were recorded in a range from 4000 cm−1 to 600 cm−1. The resolution was 2 cm−1 and 32 scans were taken for each spectrum. The evaluation was performed using Proteus and OPUS 8.1 software.
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7

Characterization of Polymer Films

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Fourier transform infrared spectrometer (FT-IR) of the films was analyzed using a VERTEX 70 (Bruker, Karlsruhe, Germany,) with a spectral range of 3500–500 cm−1. The crystalline structure was carried out on a Bruker D8 ADVANCE polycrystal X-ray diffraction (XRD, Karlsruhe, Germany) with 3 Kw output and a scanning range of 5° to 50° (2θ). Thermogravimetric analysis (TGA) was determined by using a simultaneous thermal analyzer (TG 209 F1 Libra, NETZSCH, Selb, Bavaria, Germany) at a heating rate of 10 °C/min from 30 °C to 700 °C under nitrogen atmosphere with a flow rate of 40 mL/min. The morphology of the surface and the cross-sections of the films was characterized by a Merlin scanning electron microscope (SEM, Zeiss, Oberkochen, Germany) at an accelerating voltage of 5 kV.
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8

Thermal Analysis of Organic Compounds

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Melting points (Supplementary Table 10) were determined in capillaries with a Stuart SMP 30 apparatus. TG/DTG measurements were performed with a NETZSCH TG 209 F1 Libra thermoanalyzer. The initial weights of the samples were in the range 0.6–1.6 mg. The experiments were run in an open alumina crucible in a stream of argon at a heating rate of 10 K min−1; the final temperature of these experiments was 500 °C.
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9

Comprehensive Materials Characterization Protocol

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In this study, we used a Bruker INVENIO S FT/IR spectrophotometer to measure the IR spectrum with a wavelength range of 4000–400 cm−1. Additionally, we employed a Thermo Scientific K-Alpha spectrometer to measure X-ray photoelectron spectroscopy. X-ray diffraction (XRD) spectroscopy was measured using an XRD-6000 (Shimadzu, Japan) diffractometer with a measurement range of 5°–45°. Thermogravimetric (TG) analyses of the samples were manipulated using a TG 209 F1 Libra (NETZSCH, German) analyzer heated from room temperature to 800 °C under atmosphere at the heating rate of 20 °C min−1. Nitrogen adsorption assays were conducted using a specific surface pore size analyzer (SSA-4200) after 12 hours of vacuum degassing at 313 K. The morphology of the material was observed using scanning electron microscopy (SEM, Phenom Pro). The nanoparticle size potentiometer BeNano 90 Zeta was used to measure both the zeta potential and particle size distribution. Cu elemental content was determined using an inductively coupled plasma emission spectrometry detector (ICP, 5110VDV).
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10

Thermal Behavior of Essential Oils

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The thermal behaviour of citronella oil, clove oil, lemon grass oil, their mixture and EO-MRC were evaluated using a thermal analyser (TG 209 F1 Libra®, NETZSCH-Gerätebau GmbH, 95100 Selb, Germany). Approximately about 10 mg sample weight was placed in the crucible each time. Nitrogen was used as a shielding gas. Heating program was fixed as 30–600 °C at a rate of 10 °C/min.
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