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35 protocols using labsys evo

1

Thermal Analysis of FucoPol and FucoPol HMs

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The TGA of FucoPol and FucoPol HMs was performed using thermogravimetric analyzer Setaram Labsys EVO (Setaram, Sophia Antipolis, France) in a temperature range from room temperature to 500 °C with a heating rate of 10 °C/min under an argon atmosphere. The 5% weight loss (T5%, °C) was attributed to the temperature at which the initial 5% of the mass was lost, and the thermal degradation temperature (Tdeg, °C) was assigned to the temperature value obtained for the maximum decreasing peak of the sample mass.
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2

Thermogravimetric Analysis of SEBS Polymer Nanocomposite

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The thermogravimetric analysis (TGA) was performed on a Setaram LabSys Evo (SETARAM Instrumentation, Caluire, France) instrument to analyse the SEBS polymer and SEBS/CB nanocomposite degradation. The test was carried out to quantify and verify the concentration of the carbon black filler. The composite strand was sliced into a small piece (10 mg) and placed in an Al2O3 crucible. The samples were heated in an air atmosphere (60 mL min−1) up to 1000 °C at a heating rate of 5 °C min−1.
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3

Thermal Analysis of ACN-g-ENR Samples

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TGA and DTG were performed to study the degradation temperature, mass loss, and thermal stability, as well as the compositional information, of ACN-g-ENR samples. TGA was carried out under the Setaram LABSYS EVO simultaneous thermal analyzer (Caluire-et-Cuire, France). The samples for TGA and DTG were carefully weighed in a range between ~ 7 and 9 mg in an aluminum crucible put in the center of the heating chamber. TGA was carried out in an inert environment under a nitrogen atmosphere with a temperature range from 30 to 600 °C and a heating rate of 10 °C min−1. The raw data were analyzed by the Calisto software TGA program.
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Thermal Decomposition of NIPAM-APTAC-AMPS Nanogels

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The thermal decomposition of the NIPAM-APTAC-AMPS nanogels was investigated using a LabSys Evo (Setaram, Caluire-et-Cuire, France) under a nitrogen atmosphere in a temperature range of 25 to 500 °C, with a heating rate of 10 °C min−1. The TG curve made possible the determination of the initial decomposition temperature and the residual mass percentage. Further, the maximum thermal decomposition temperature of the NIPAM-APTAC-AMPS nanogels was calculated using the differential peaks of the DTA curve.
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5

Physiochemical Characterization of Novel Materials

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Powder X-ray diffraction (PXRD) patterns of all obtained samples were recorded in the 2θ range of 5–40° on an X-ray diffractometer (X-Pert PRO, PANalytical) at 40 kV, 40 mA with Cu-Kα radiation (λ = 0.15406 nm). Thermogravimetric analyses (TGA) were performed on a TA analyzer (Labsys Evo, Setaram) under air atmosphere, in which the TG profiles were collected from 50 to 800 °C at a rate of 10 °C min−1. Fourier transform infrared (FTIR) spectra of all samples were detected on a Nicolet iS50 Fourier transform infrared spectrometer. The texture properties were measured by Argon adsorption at 87 K with the Autosorb iQ physical adsorption instrument (Quantachrome Instruments, Boynton Beach, Florida, USA), and the characterization details were shown in the ESI S1.
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6

Thermal Analysis of Material Samples

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Differential scanning calorimetry (DSC) analysis was performed in a DSC Q2000 from TA Instruments Inc. (Tzero DSC technology, New Castle, DE, USA) operating in the Heat Flow T4P option. The measurements were carried out under anhydrous high purity nitrogen at a flow rate of 50 mL/min. DSC Tzero calibration was carried out in the temperature range from −90 to 200 °C. The samples were submitted to two cooling and heating runs between −90 and 120 °C, at a rate of 10 °C/min. The samples were encapsulated in Tzero (aluminium) hermetic pans with a Tzero hermetic lid, without a pinhole to avoid water loss by evaporation.
Thermogravimetric analysis (TGA) was performed with a Labsys EVO (Setaram, Caluire, France). The samples were placed in an aluminum pan and analyzed in a temperature ranging between 25 and 500 °C, using a heating rate of 10 °C/min.
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7

Thermal Behavior Profiling of Collagen

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To evaluate the thermal behavior profiles of the collagen extracts, TGA analysis was performed in a Thermal Analysis instrument (Labsys EVO, Setaram, Caluire, France), in an argon atmosphere, within a temperature range between 25 and 700°C and a 10°C/min heat ramp.
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8

Comprehensive Materials Characterization Protocol

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The powder X-ray diffraction (XRD) patterns were recorded by a Rigaku Ⅱ X-ray diffraction spectrometer (Japan Science Co., Tokyo, Japan) using Cu-Kα radiation. Fourier-transform infrared (FTIR) transmission spectra were performed by FTIR-65 IR spectrophotometer (Tianjin Port East Technology Co., Tianjin, China). Thermogravimetric–Differential Thermal Analysis (TG-DTA) was performed by a Labsys Evo thermogravimetric differential thermal analyzer from the Setaram Instrumentation (France) with a rate of 10 K min−1 under ambient condition. The JSM-JSM7500 instrument (Japan Electronics Co., Tokyo, Japan) obtained scanning electron microscopy (SEM) images. X-ray photoelectron spectroscopy (XPS) was taken on the PHI5000VersaProbe instrument (Shanghai Yuzhong Industrial Co., Shanghai, China). Inductively Coupled Plasma–Atomic Emission Spectrometry (ICP-AES) record was obtained by ICP-9000(N+M) atomic emission spectroscopy (Thermo Jarrel-Ash Co., Boston, MA, USA).
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9

Thermal Analysis of Drug Samples

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The small amount of the tested drug (below 10 mg) was located in an aluminum crucible with a lid and heated to a temperature of 450 °C under an argon atmosphere, using a heating rate of 5 °C/min. The LabsysEvo (Setaram Inc., Cranbury, NJ, USA) apparatus was used for the thermal analysis. For every sample, the measurement was performed under the same conditions.
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10

Thermogravimetric Analysis of Materials

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Thermogravimetric analysis (TGA) was performed using Labsys EVO thermogravimetric equipment (Setaram, Caluire-et-Cuire, France) with a temperature range from 30 to 600 °C and a heating rate of 10 °C min−1 in a nitrogen atmosphere (N2 flow rate = 40 mL min−1) [15 (link)].
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