## Abstract The products and mechanism of the thermal oxidative degradation of poly(ethylene oxide) at 150βΒ°C have been analysed using ^13^C NMR spectroscopy. The analysis was assisted by the use of distortionless enhancement by polarisation transfer spectra, longitudinal relaxation time measuremen
A study of the mechanism of the oxidative thermal degradation of poly(ethylene oxide) and poly(propylene oxide) using 1H- and 13C-NMR
β Scribed by Li Yang; Frank Heatley; Trevor G. Blease; Robert I.G. Thompson
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 946 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
The oxidative thermal degradation of poly(ethylene oxide) (PEO) and poly(propylene oxide) (PPO) at 150Β°C in air was studied. The weight loss was determined, and the structure of the residual polymer investigated using NMR. In PEO, the only significant structural changes were the formation of formate ester and hydroxy end-groups, the former predominating. In PPO, significant amounts of primary hydroxy end-groups of the structure -OCH(CH,)CH,OH and secondary hydroxy end-groups of the structure -CH,CH(CH,)OH were formed, together with their formate and acetate esters. These structural changes have been interpreted in terms of the decomposition of a peroxy species initially formed by substitution of a backbone hydrogen by a peroxy group.
π SIMILAR VOLUMES
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TGA curves for the thermal decomposition of PS in nitrogen (dashed line) and air (solid line). Heating rates of 9.0 and 8.2 K N min -1 for nitrogen and air, respectively.