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Tga dsc 3 thermogravimeter

Manufactured by Mettler Toledo
Sourced in Switzerland

The TGA/DSC 3+ thermogravimeter is a laboratory equipment designed for thermal analysis. It measures the change in a sample's weight as a function of temperature or time under a controlled atmosphere. The core function of this instrument is to provide quantitative information about physical and chemical changes in materials, such as decomposition, oxidation, and phase transitions.

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2 protocols using tga dsc 3 thermogravimeter

1

Thermal Stability Analysis of Dried Samples

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The thermal stability and decomposition characteristics of the dried samples were analyzed using a TGA/DSC 3+ thermogravimeter (Mettler Toledo, Greifensee, Switzerland). Approximately 5 to 7 mg of the material was weighed into 70 µl aluminium oxide crucibles and subjected to heating from 30 to 600 °C at a rate of 5 °C/min in a nitrogen atmosphere (50 ml/min) [35] (link). The TG and DTG curves were derived from the differential values of the mass loss with respect to temperature. Thermograms (TGA/DTG) were assessed using the STAR software (version 16.10) from Mettler Evaluation. Each sample underwent two replicates for robust analysis.
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2

Characterization of Surface-Modified Magnetic Nanoparticles

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FTIR measurements were carried out in Attenuated Total Reflectance (ATR) mode using the Nicolet iS10 apparatus with an adapter equipped with a diamond crystal (Thermo Scientific). Measurements were carried out in the mid-infrared range (500–4000 cm−1) using: (i) solid samples of nanoparticle powders and (ii) surface modifiers in their pure form. Thermogravimetric analysis (TGA) was carried out using a TGA/DSC3+ thermogravimeter (Mettler Toledo) at a temperature increment 10 °C/min in a temperature window of 25–750 °C and air flow rate 60 mL/min. The total content of C, H, and N elements in modified MNPs was measured using a Vario EL III analyzer with a thermal conductivity detector (Elementar, Langenselbold, Germany) by the accurate weighting of the solid sample and its burning in oxygen at 1150 °C in a dynamic system. Fe, Au, and Si content in solid MNPs was established using the ICP-MS/MS technique, analogically to the methodology presented above (see Section 3.3.2; monitored isotopes: 28Si, 56Fe, 197Au at on-mass mode), but solid samples before digestion were accurately weighted. The oxygen content in the cores of surface-modified MNPs was estimated using the molar ratio of Fe/O in the synthesized bare MNPs as the rest types of the nanomaterials were formed based on such cores (with specific FeO/Fe2O3 ratio).
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