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Thermal degradation kinetics and mechanism of epoxidized natural rubber

  • Canzhong He , Yueqiang Wang , Yongyue Luo , Lingxue Kong EMAIL logo and Zheng Peng EMAIL logo
Published/Copyright: May 15, 2013
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Abstract

Thermal resistance is one of the most dominative properties for polymer materials. Thermal degradation mechanisms of epoxidized natural rubber (ENR) and NR are studied by thermogravimetric analysis (TGA) and differential thermal analysis (DTA). The results show that, the introduction of epoxy groups into the NR molecular main chain leads to a remarkable change in the degradation mechanism. The thermal stability of ENR is worse than that of NR. For the first thermooxidative degradation stage, the thermal decomposition mechanism of ENR is similar to that of NR, which corresponds to a mechanism involving one-dimensional diffusion. For the second stage, the thermal decomposition mechanism of ENR is a three-dimensional diffusion, which is more complex than that of NR. Kinetic analysis showed that activation energy (Eα), activation entropy (ΔH) and activation Gibbs energy (ΔG) values are all positive, indicating that the thermooxidative degradation process of ENR is non-spontaneous.


Corresponding authors: Lingxue Kong, Institute for Frontier Materials, Deakin University, Waurn Ponds Vic 3216, Australia; and Zheng Peng, Agricultural Product Processing Research Institute, Chinese Academy of Tropical Agricultural Sciences, Zhanjiang 524001, China; and Institute for Frontier Materials, Deakin University, Waurn Ponds Vic 3216, Australia

The financial support from the National Program on Key Basic Research Project of China for 973 Program (contract grant number: 2010CB635109) is gratefully acknowledged.

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Received: 2013-2-24
Accepted: 2013-4-7
Published Online: 2013-05-15
Published in Print: 2013-07-01

©2013 by Walter de Gruyter Berlin Boston

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