Q50 thermogravimetric analyzer
The Q50 thermogravimetric analyzer is a laboratory instrument designed to measure the change in the mass of a sample as a function of temperature or time. It is used to analyze the thermal stability and composition of materials.
Lab products found in correlation
44 protocols using q50 thermogravimetric analyzer
Thermal Stability of Polylactic Acid
Thermogravimetric Analysis of Samples
Quantifying Polymer Content in Microgels
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.
Thermal and Spectral Analysis of Materials
Thermal Stability Assessment of Composite Films
Thermal Analysis of Polymer P1
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.
Characterization of GlcNAc-Functionalized Silica Sorbent
Quantifying Mineral Composition in Shells
Thermal Stability Analysis by TGA
Nanoparticle Surface and Structural Characterization
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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