Mechanical and thermal degradation behavior of high-performance PDMS elastomer based on epoxy/silicone hybrid network
In this study, the high-performance PDMS elastomer was successfully prepared by constructing epoxy/silicone hybrid network through hydrosilylation and epoxide-opening reaction. The tensile strength, elongation at break and shear strength of the prepared hybrid material were increased by 200.0%, 59.6...
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Published in | Polymer (Guilford) Vol. 236; p. 124299 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
30.11.2021
Elsevier BV |
Subjects | |
Online Access | Get full text |
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Summary: | In this study, the high-performance PDMS elastomer was successfully prepared by constructing epoxy/silicone hybrid network through hydrosilylation and epoxide-opening reaction. The tensile strength, elongation at break and shear strength of the prepared hybrid material were increased by 200.0%, 59.6%, 140.6% respectively when compared with the pure PDMS. The thermal residual weight of the hybrid material at 800 °C in N2 was kept at 56.9%. The thermal degradation mechanism of hybrid material was investigated through TG-IR analysis. Friedman technique was used to compute the kinetic parameters of degradation reaction. Meanwhile, the composition and structure of residual char of hybrid material after thermal degradation at 800 °C was systematically characterized. Results indicated that the high-performance PDMS elastomer with excellent thermal and mechanical properties was expected to be applied in many prospects such as thermal protective coating, high temperature resistant adhesive and ablative material matrix.
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•A novel epoxy/silicone hybrid network was constructed.•Mechanical and adhesive properties of the hybrid materials were improved.•Thermal properties of the hybrid materials were maintained at a high level.•Thermal degradation mechanism of hybrid material was discussed in detail.•Thermal degradation residual char of hybrid material was studied in detail. |
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ISSN: | 0032-3861 1873-2291 |
DOI: | 10.1016/j.polymer.2021.124299 |