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Tga q50 thermal analyzer

Manufactured by TA Instruments
Sourced in United States

The TGA Q50 Thermal Analyzer is a laboratory instrument designed to measure the weight changes of a sample as a function of temperature or time. It provides precise and accurate data on the thermal stability, composition, and decomposition characteristics of materials. The TGA Q50 can operate across a wide temperature range and supports various sample types and environments.

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2 protocols using tga q50 thermal analyzer

1

Thermal Stability Analysis of Films

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Thermogravimetric analysis was used to investigate the mechanism of decomposition and thermal stability. The films were subjected to heating rates of 30 °C/min from 25 °C to 1000 °C in air and nitrogen in a TGA Q50 Thermal Analyzer purchased from TA Instruments, New Castle, DE, USA.
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2

Comprehensive Physicochemical Characterization of Lignin-based Copolymers

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For FTIR analysis, The KBr pressed disc technique (2–4 mg of sample and 200 mg of KBr) was used. Data acquired in Shimadzu 8400 FT-IR spectrophotometer. Absorbance spectra were obtained from 4000 to 400 cm-1 with a 4 cm-1 resolution, Background spectra were also collected and subtracted. The 1H spectra were taken on a Bruker DPX200 (500 MHz for 13 C and 200 MHz for 1 H) in D2O solvent using tetramethylsilane (TMS) as an internal standard. Both cases 5 mg/mL concentrated solutions were prepared. All signals were referenced to TMS within ± 0.1 ppm. The thermo oxidative stability of pure lignin and lig-g-POZ with different weight (%) lignin content copolymer were carried out using a TGA Q50 thermal analyzer of TA Instruments, USA. All the experiments were performed by heating the sample at a rate of 10 °C/min, in nitrogen atmosphere, from room temperature to 600 °C. DSC studies of the pure lignin and lig-g-POZ copolymer with different weight (%) lignin content were performed using a DSC Q100, of TA instruments make, USA. Approximately 10 mg of the samples was placed in an aluminum crimple and sealed with the help of a hand press prior to placing it on the sample platform of the instrument. The scanning was carried out in the temperature range of 30 °C to 200 °C at a heating rate of 10 °C/min in a stream of continuous supply of dry nitrogen.
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