Non-isothermal decomposition kinetics of commercial polyacrylamide hydrogel using TGA and DSC techniques

•The thermal decomposition of commercial polyacrylamide hydrogel (CPH) is studied.•The non-isothermal decomposition kinetics of CPH was performed using TGA and DSC.•Malek and Vyazovkin methods used to determine kinetic parameters of CPH.•Thermal decomposition releases ammonia and CO2 are released in...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Thermochimica acta 2023-07, Vol.725, p.179532, Article 179532
Hauptverfasser: Zamani-Babgohari, Fatemeh, Irannejad, Ahmad, Khayati, Gholam Reza, Kalantari, Maryam
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•The thermal decomposition of commercial polyacrylamide hydrogel (CPH) is studied.•The non-isothermal decomposition kinetics of CPH was performed using TGA and DSC.•Malek and Vyazovkin methods used to determine kinetic parameters of CPH.•Thermal decomposition releases ammonia and CO2 are released in two stages.•The Sestak-Begren model can describe several aspects of the study. The thermal decomposition method was employed to analysis the non-isothermal kinetics of commercial polyacrylamide hydrogel. Malek model-based methods and Vyazovkin model-free advanced converter methods were used to analyze the non-isothermal kinetics of hydrogel decomposition using DSC and TGA data. Thermal decomposition takes place in two stages. FTIR diagrams showed that ammonia gas and CO2 were likely released during the first and second stages of decomposition, respectively. By breaking the main chain in the second stage, the polymer loses a significant amount of weight. The Sestak-Berggren model describes the reaction process. The activation energies for the first and second stages were calculated to be (40±3 kJ/mol) and (59±3 kJ/mol), respectively. Finally, a commercial polyacrylamide hydrogel decomposition explicit rate equation was derived. The increase in surface porosity with the progress of the degradation process can be evidence of autocatalysis effects.
ISSN:0040-6031
1872-762X
DOI:10.1016/j.tca.2023.179532