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39 protocols using sta 449 f1 jupiter

1

Thermal Decomposition Analysis of Materials

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The TG/DTG analyses for the tested materials were performed using a STA 449 Jupiter F1 instrument produced by Netzsch, Selb, Germany. Ten milligrams (10 mg) of the sample was put into an Al2O3 crucible and heated between the temperatures of 40 °C and 550 °C with a heating rate of 10 K min−1 in the presence of a helium atmosphere (a flow rate of 40 mL min−1). The initial decomposition temperatures (T5%), maximum decomposition temperatures (Tmax), and mass losses (Δm) at each stage of the decomposition and the residual masses at 550 °C (rm) were determined.
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2

Thermal Analysis of MCF-LYS Adsorption

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The thermal analysis was used to examine the thermal stability, behavior, and decomposition of the MCF materials before and after LYS adsorption, as well as to determine the presence of protein on the silica surface or in the pores. The thermal experiment was carried out on the apparatus STA 449 Jupiter F1 (Netzsch, Selb, Germany). The samples (~18 mg) in aluminum crucibles were heated in the temperature range 30–950 °C with a heating rate of 10 °C/min under a dynamic atmosphere of synthetic air with a flow rate of 50 mL/min. The sensor thermocouple type S TG-DSC and empty Al2O3 crucible as a reference were used. The identification of gas products emitted during decomposition of the studied materials was detected and analyzed by quadrupole mass spectrometer QMS 403C Aëolos (Netzsch, Selb, Germany) and Fourier transform infrared spectroscopy FTIR spectrometer Brucker (Ettlingen, Germany) coupling on-line to STA instrument. The QMS data were collected in the range of 10 to 300 amu. The FTIR spectra in the spectral range 600–4000 cm−1 with 16 scans per spectrum at a resolution 4 cm−1 were recorded.
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3

Thermal Analysis of Activated Carbons

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Thermal analysis of activated carbons was conducted using a STA 449 Jupiter F1 instrument, (Netzsch, Selb, Germany). The measurements in synthetic air atmosphere (50 cm3/min) at a temperature range of 30 to 1200 °C (heating rate 10 °C/min) were carried out. The standard Al2O3 crucible and thermocouple of type S as TG-DSC sensor were applied. The gaseous products released during decomposition of samples were analyzed by FTIR spectrometer (Bruker, Ettlingen, Germany) and by quadrupole MS spectrometer QMS 403C Aeölos (Netzsch, Selb, Germany) coupled on-line to STA instrument.
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4

Thermal Analysis of PVA Cryogels

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To characterize the thermal behavior of PVA as well as PVA_PEBSA cryogel samples, thermogravimetric analysis was performed on a Jupiter STA 449 F1 thermobalance produce by Netzsch (Selb, Germany). Freeze dried samples with a weight between 10 and 12 mg was placed in Al2O3 crucibles and heated from room temperature up to 675 °C in dynamic mode with a heating rate of 10 °C/min and 40 mL/min nitrogen flow. The data obtained were subsequently processed using Proteus Analysis software.
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5

TG-DSC Analysis of Thermal Behavior

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TG-DSC analysis was carried out using a Jupiter STA 449 F1 instrument (Netzsch, Selb, Germany). The analysis was performed with a heating rate of 10 °C/min and a maximum temperature of 1000 °C. Measurements were conducted under a constant flow of helium (40 cm3/min). The sample mass was approximately 30 mg. The volatile products evolved during heating were detected by a 403C Aëolos mass spectrometer (QMS, Selb, Germany) coupled online to the STA instrument. The QMS was operated with an electron impact ionizer with an energy of 70 eV. During the measurements, the m/z ratio was recorded in the range of 2–150 amu, where m is the mass of the molecule and z its charge.
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6

Thermogravimetric Analysis of Nanoparticles

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Thermogravimetric analysis was carried out on dried nanoparticles using an online TG-DSC/FT-IR/MS system. The system is equipped with an apparatus of simultaneous thermogravimetric and differential scanning calorimetry analyses model STA 449F1 Jupiter (Netzsch, Selb, Germany), FT-IR spectrophotometer Vertex-70 model (Bruker-Germany) and mass spectrometer QMS 403C Aëolos model (Netzsch, Selb, Germany). The samples were heated under a nitrogen flow with a 50 mL/min−1 rate in an open Al2O3 crucible. Analyses were performed in dynamic mode at a heating rate of 10 °C/min from room temperature up to 600 °C. Data collection was realized with Proteus® software.
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7

Thermal Decomposition Analysis of PLA/HAp Biocomposites

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The thermal decomposition of the PLA/HAp composite in the form of freeze-dried pellets, custom extruded biocomposite filament and PLA/HAp composite print as well as the reference PLA samples, were analysed with the use of STA 449 F1 Jupiter (Netzsch Instruments, Germany). 10–20 mg of samples were placed in ceramic cups and heated from 30 °C up to 1350 °C at a heating rate of 10 °C min−1 under an air flow of 40 mL min−1.
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8

Thermogravimetric Analysis of Samples

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Use Netzsch Instruments model STA449 F1 Jupiter for TGA measurement. Place the sample (5–8 mg) in Al-pan in N2 atmosphere, the temperature range is 30–400 °C, and the heating rate is 10 °C/min.
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9

Thermal Analysis of Coated Samples

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Thermal analysis of the uncoated and sol–gel coated samples was conducted by thermogravimetric analysis (TGA) using equipment STA 449 F1 Jupiter (Netzsch, Germany). The samples were heated at a rate of 10 K min−1 from 25 to 800 °C under nitrogen atmosphere purged at 30 ml min−1 using an alumina crucible.
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10

DSC Analysis of Material Samples

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Samples for DSC analysis were cut using the wire-cutting machine. The input weight of the samples was 20 mg. The DSC analysis was performed with a heating rate of 30 K/min in a nitrogen atmosphere using the simultaneous thermal analyzer, a STA 449 F1 Jupiter (Netzsch, Waldkraiburg, Germany).
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