Thermal degradation of polydimethylsiloxane (PDMS) polymers having hydroxyl (PS) and vinyl (PS-V) terminals was studied by pyrolysis-gas chromatography (PGC) in the temperature range from 550 to 950°C. The degradation products were primarily cyclic oligomers ranging from trimer (D 3 ) to cyclomer D
Strategy for kinetic parameter estimation—Thermal degradation of polyurethane elastomers
✍ Scribed by Ante Agić; Emi Govorĉin Bajsić
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 356 KB
- Volume
- 103
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
Abstract
The kinetics of the thermal degradation of polyurethane (PU) elastomers based on poly(ether polyol) soft segments and an aromatic type of diisocyanate were investigated by thermogravimetric analysis (TGA) under a nitrogen atmosphere employing four heating rates. The corresponding kinetic parameters of the two degradation stages were estimated by minimizing the output error functional and by the Kissinger method. In evaluating the kinetic parameters of the two‐step PU thermal decomposition, a differential thermogravimetry curve was applied as an objective functional in a regression procedure. Parameter estimation was obtained by minimizing the weighted quadratic output error functional with the modified Nelder–Mead simplex search algorithm. The confidence regions in the preexponential factor‐activation energy space were established for both the first and second stages of degradation. The effect of the molecular weight of the soft segment and the content of the hard segment on the activation energy of the degradation process was constructed by response surface methodology. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 764–772, 2007
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