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44 protocols using q50 thermogravimetric analyzer

1

Thermal Stability of Polylactic Acid

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Additionally, a thermogravimetric analysis (TGA) was performed to identify the thermal stability of PLA samples using the Thermogravimetric analyzer Q50 from TA instruments Inc. (USA). Approximately 15 mg of polymer were heated from 30 to 430 °C at 10 °C/min, under N 2 flow at 10 mL/min. A temperature of 5% wt. mass loss (Tloss5%) was determined.
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2

Thermogravimetric Analysis of Samples

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Thermogravimetric characterization was performed using a Thermogravimetric Analyzer Q50 (TA Instruments, New Castle, DE, USA). Samples of 5–15 mg were isothermally stabilized at 25 °C for 5 min, heated from 25 to 600 °C, at a heating rate of 10 °C/min, under a N2 purge flow of 5 mL/min.
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3

Quantifying Polymer Content in Microgels

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1 mL of the microgel suspensions was transferred to microcentrifuge
tubes. The tubes were centrifuged at 20,000 rcf for 1 h at room temperature.
To ensure samples were not compressed during analysis, the microgel
pellets were allowed to recover their shape overnight at room temperature.
The supernatant was then decanted from the microgel samples. About
10–30 mg of the pellet was transferred to a ceramic dish that
was placed on a platinum pan. The sample was then loaded into a TA
Instruments Q50 Thermogravimetric Analyzer and subjected to a linear
ramp from 40 to 600 °C at 10 °C min–1 under
a constant flow of nitrogen at 20 mL min–1. The
concentration of polymer in the packed microgel pellets was determined
as the relative weight associated with polymer decomposition in the
thermogram (occurring around 350–425 °C) to the total
weight of the sample. At least three samples were analyzed per microgel
formulation.
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4

Thermal and Spectral Analysis of Materials

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Thermal gravimetric analysis was performed on the TA instruments Q50 Thermogravimetric Analyzer, in the temperature range from 25 to 500 °C, at a heating rate of 2 or 5 °C min−1. Infrared (IR) spectra were acquired in the range of 4000–400 cm−1 using JASCO 6800 FT-IR spectrometer.
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5

Thermal Stability Assessment of Composite Films

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The thermal stability of p-WCT, MCNTs, and cellulose/MCNT composite films in nitrogen atmosphere was evaluated using a Q50 thermogravimetric analyzer (TA, United States). Heating speed of 15 °C/min and 5 mg film samples were used. The curves ranging from 50 °C to 800 °C were displayed.
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6

Thermal Analysis of Polymer P1

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We characterized bulk material thermal properties of P1 via differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). DSC was conducted using a DSC-Q100 (TA Instruments). Raw P1 (5 mg) was hermetically sealed into an aluminum sample pan (TA instruments) and subjected to a 10 °C/min heating/cooling cycle from −80 °C to 200 °C and back to −80 °C, which was repeated twice. The data in Fig. 4 are the final heating scan.
TGA was conducted using a Q50 Thermogravimetric Analyzer (TA Instruments). Raw P1 was placed in an alumina crucible and subjected to a 10 °C/min temperature ramp under N2 up to 800 °C. All DSC and TGA data were analyzed using TA Universal Analysis software.
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7

Characterization of GlcNAc-Functionalized Silica Sorbent

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All HPLC separations were performed using Waters Alliance 2629 separation module (Milford, MA, USA), connected with an in-line degasser, a quaternary solvent pump, an autosampler, and a thermostated column compartment. A Waters PDA detector (model 2475) was used to record the signals at 254 nm. All the chromatographic separations were carried out by maintaining the column at room temperature. N-Acetylglucosamine functionalized-silica (GlcNAc-silica) slurry was packed in stainless-steel columns using a constant pressure pump from Shandon Southern Products Ltd. (Rincon, Cheshire, UK). Data acquisition was performed using Empower 2 (Build 2154) software (Waters Chromatography), and then the offline chromatographic data were processed using OriginPro v8.5.1 (Origin Lab Corp., Northhampton, MA, USA). Fourier transform infrared (FTIR) analyses were carried out for the characterization of GlcNAc-silica sorbent using attenuated total reflectance mode on a Nicolet IS50 FT-IR instrument from Thermo Scientific Co. (Waltham, MA, USA). Furthermore, the functionalization of silica with surface bound N-acetylglucosamine was assessed via thermogravimetric analysis using a Q-50 thermogravimetric analyzer from TA instruments (New Castle, DE, USA). Approximately 8–10 mg of the samples was heated from 20 °C to 900 °C at a heating rate of 20 °C per min with a 40 mL/min continuous nitrogen gas flow.
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8

Quantifying Mineral Composition in Shells

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Thermogravimetric analysis was performed on a Q50 thermogravimetric analyzer (TA Instruments) to quantify the principal minerals in the shells, using a heating protocol of 10°C min−1 up to 900°C in a nitrogen atmosphere at 70 mL min−1. To this end, the material was dissolved in chloroform and the resulting supernatant and sediment were analyzed separately.
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9

Thermal Stability Analysis by TGA

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Thermogravimetric analyses (TGA) for studying thermal stability at relatively low temperatures (<600 °C) were performed at a heating rate of 20 °C/min (sample weight ca. 5 mg) with a Q50 thermogravimetric analyzer of TA Instruments and under a flow of dry nitrogen. Test temperatures ranged from 50 to 600 °C.
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10

Nanoparticle Surface and Structural Characterization

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The amount of surfactant remaining on the
nanoparticle surface was determined using a Q50 thermogravimetric
analyzer (TA Instruments, Inc., New Castle, DE) under air injection
with a heating rate of 5 °C/min up to 800 °C. The surface
area (SBET) of nanoparticles was estimated
by nitrogen physisorption at −149 °C using a Gemini VII
2390 Surface Area Analyzer (Micromeritics, GA, United States). The SBET values were determined following the BET
method.65 (link)The hydrodynamic diameter
of the nanoparticles was obtained by DLS measurements using a NanoPlus-3
(Micromeritics, USA) after sonication for 6 h at 25 °C. The zeta
potential was determined by electrophoretic light scattering to determine
the dispersion of nanoparticles in the aqueous phase using the NanoPlus-3
(Micromeritics, USA).66 (link),67 (link)Functional groups over
the surface of the nanomaterials were characterized by FTIR spectroscopy
with an IRAffinity spectrophotometer (Shimadzu, Japan). Each sample
was diluted with KBr at a 1:3 mass ratio. For sample detection, a
KCl cell with a 0.25 mm spacing was used and placed in the FTIR at
25 °C with 20 sweeps per minute for each sample in a range of
4000 to 500 cm–1 at a resolution of 2 cm–1.
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