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Tga dsc1 apparatus

Manufactured by Mettler Toledo
Sourced in United States

The TGA/DSC1 apparatus is a thermal analysis instrument that combines thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) capabilities. It is designed to measure the changes in a sample's mass and thermal properties as a function of temperature or time under a controlled atmosphere.

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5 protocols using tga dsc1 apparatus

1

Thermal Decomposition Analysis by TGA

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Thermogravimetric analysis (TGA) measurements were performed by means of a TGA/DSC1 apparatus (Mettler Toledo, Greifensee, Switzerland) equipped with STAR software. The experiments were carried out under air flow (40 mL min−1) at the temperature range from 25 to 850 °C with a heating rate of 5 °C min−1.
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2

Polymer Characterization by NMR and SEC

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The 1H and 13C NMR spectra were recorded on a Bruker AVANCE 400 or on Bruker Avance III (600 MHz) spectrometers (Bruker Corporation, Billerica, MS, USA). CDCl3 (Cambridge Isotope Laboratories, Inc., Tewksbury, MA, USA, D 99.8%) was used as purchased. The chemical shifts are reported in ppm relative to the solvent residual peaks.
Size exclusion chromatography (SEC) of polymer samples was performed using an Agilent PL-GPC 220 chromatograph equipped with a PLgel column (Agilent Technologies, Santa Clara, CA, USA) and THF was used as the eluent (1 mL/min). The measurements were recorded with universal calibration based on a polystyrene standard at 40 °C.
Differential scanning calorimetry (DSC) experiments were performed on the TGA/DSC1 apparatus (Mettler Toledo, Columbus, OH, USA).
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3

Thermal Analysis of Samples

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Thermal analysis (thermogravimetry and differential scanning calorimetry) were carried out simultaneously using TGA/DSC1 apparatus (Mettler Toledo, Columbus, OH, USA). Samples were fractioned, weighed (not less than 10 mg) and placed into 100 µL aluminum crucibles. The analyses were performed at an air atmosphere in a temperature range from 30 to 600 °C, with a heating rate of 10 °C per minute.
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4

Thermal Analysis of Graphene Oxide Composites

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Thermogravimetric analysis (TGA) was carried out on the composites and GO samples using a TGA/DSC 1 apparatus (Mettler Toledo, UK). A sample of the freeze-dried GO was thermally reduced according to the cure schedule employed for processing the composites (i.e. 90 °C for 1 h; 160 °C for 2 h and 200 °C for 30 min). To investigate the thermally induced dissociation of the GO and rGO, samples were analysed in a nitrogen atmosphere using a heating rate of 5 °C/min. Thermal oxidation of the composites, on the other hand, was analysed in air using a heating rate of 10 °C/min. All samples were analysed over the temperature range 30–800 °C.
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5

Characterization of Nanomaterial Morphology

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The morphology and size of the products were obtained using scanning electron microscopy (SEM) with a JSM-6510A microscope and by sputtering with gold. The samples were examined by X-ray diffraction (XRD-7000), recorded using a Shimadzu X-ray powder diffractometer with Cu-Kα radiation (λ = 0.15405 nm). X-ray photoelectron spectroscopy (XPS, ESCALAB-250) with an Al-Kα radiation source were used. Chemical bonding information of the studied samples was gathered with Fourier transformed infrared spectroscopy (FTIR, Nicolet iS50). Thermogravimetric analysis (TG) was carried out using MettlerToledo TGA/DSC1 apparatus.
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