4.5 Article

Insights into self-healing performance of epoxidized deproteinized natural rubber/graphene oxide composite

Journal

POLYMER ENGINEERING AND SCIENCE
Volume 63, Issue 6, Pages 1781-1791

Publisher

WILEY
DOI: 10.1002/pen.26324

Keywords

epoxidized deproteinized natural rubber; graphene oxide; hydrogen bonds; interdiffusion; self-healing

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This study investigated the self-healing performance of epoxidized deproteinized natural rubber (EDPNR) and EDPNR/graphene oxide (GO) composites. It was found that the recovery of tensile strength was higher for EDPNR25/GO0.5 and EDPNR25/GO1.0 composites compared to EDPNR50/GO0.5 and EDPNR50/GO1.0 composites. The interdiffusion of epoxidized natural rubber molecules was identified as the key factor affecting the self-healing performance rather than the hydrogen bonds between GO and functional groups on EDPNR molecules.
The self-healing performance of epoxidized deproteinized natural rubber (EDPNR) and EDPNR/graphene oxide (GO) composites was investigated. Composites of EDPNR25 and EDPNR50 with GO contents of 0.5 and 1.0 phr were prepared by adding a GO dispersion into a EDPNR latex and the product was subsequently cast into films. Tensile strengths of the original samples and after self-healing were used to evaluate self-healing performance. The tensile strength of EDPNR25 after self-healing achieved about 65% of tensile strength of original EDPNR25. The recovery of tensile strength for the composite increased to 81% for EDPNR25/GO0.5 and 105% for EDPNR25/GO1.0 for self-healing at 25 degrees C for 24 h. At 70 degrees C, EDPNR25/GO0.5 and EDPNR25/GO1.0 composite achieved similar to 100% recovery after 24 h. On the other hand, the tensile strength recoveries of EDPNR50, EDPNR50/GO0.5, and EDPNR50/GO1.0 were relatively low (33%, 28%, and 24%, respectively) at 25 degrees C. At 70 degrees C, recoveries increased to 63%, 67%, and 52%, respectively. This result demonstrated that the interdiffusion of epoxidized natural rubber molecules plays a key role in the self-healing performance rather than hydrogen bonds between GO and functional groups on EDPNR molecules.

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