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Enzymatic degradation, electronic, and thermal properties of graphite‐ and graphene oxide‐filled biodegradable polylactide/poly(ε‐caprolactone) blend composites
Author(s) -
Botlhoko Orebotse Joseph,
Makwakwa Dimakatso,
Ray Suprakas Sinha,
Ramontja James
Publication year - 2019
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.47387
Subject(s) - materials science , composite material , graphene , graphite oxide , oxide , crystallization , graphite , thermal conductivity , caprolactone , electrical resistivity and conductivity , polymer , chemical engineering , copolymer , nanotechnology , electrical engineering , engineering , metallurgy
Commodity polymers are the most widely used materials for electronic packaging applications. However, they are nondegradable and causing serious environmental damage. Addressing this challenge, the relative effects of graphite (G) and graphene oxide (GO) dispersion on the enzymatic degradation, electronic properties, thermal degradation, and crystallization behavior of enzyme degradable polylactide/poly(ε‐caprolactone) blend composites is investigated. Owing to the oxygenated surface functionalities and excellent thermal conductivity arising from the carbon structure, the randomly dispersed GO particles do not provide electrical pathways and facilitate large enhancements in the electrical resistivity (126%) and thermal conductivity (72%) of the blend composites. However, while the G particles enhanced the thermal conductivity of the composites, they had little effect on enzymatic degradation. Furthermore, they reduced the electrical resistivity, particularly at high concentration (0.25 wt % G), as a result of the conducting delocalized electrons in the G structure and due to network formation. We also find that the energy required to initiate and propagate the thermal degradation process for GO‐filled blend composites is relatively lower than that of G‐filled blend composite. However, the former composites show higher crystallization rate coefficients value than that of G‐filled composites and the neat blend, thereby providing better crystallization ability and miscibility with the matrix. In summary, the GO‐filled blend composites are observed to show potential for use in sustainable materials for thermal management applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 47387.