Loading…
The effect of molecular chain polarity on electric field-induced aligned conductive carbon nanotube network formation in polymer melt
Two ethylene–vinyl acetate (EVA) copolymers containing 10 and 25wt.% vinyl acetate (EVA10 and EVA25) were utilized to explore the effect of molecular polarity on the formation of conductive carbon nanotube (CNT) network in EVA melt under an electric field. Because of the different interfacial energy...
Saved in:
Published in: | Composites science and technology 2012-10, Vol.72 (15), p.1875-1881 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Two ethylene–vinyl acetate (EVA) copolymers containing 10 and 25wt.% vinyl acetate (EVA10 and EVA25) were utilized to explore the effect of molecular polarity on the formation of conductive carbon nanotube (CNT) network in EVA melt under an electric field. Because of the different interfacial energy, it was supposed to be stronger molecular chain-CNT interaction in CNT/EVA25 than that in CNT/EVA10. The critical time for conductive CNT network formation decreased with annealing temperature, filler loading and EVA polarity. The activation energy of conductive CNT network formation (93.9kJ/mol) in CNT/EVA10 is lower than that (104.7kJ/mol) in CNT/EVA25. By a thermodynamic percolation model, the percolation threshold at the equilibrium state was about 0.19vol.% for CNT/EVA10, while it rose to 0.27vol.% for CNT/EVA25. Morphological observation showed a high degree of CNT alignment in CNT/EVA10 compared to CNT/EVA25 after application of an electric field. The results suggested the strong CNT–EVA chain interaction and higher viscosity of polymer matrix limited the CNT alignment and the conductive network tended to form easily in EVA melt with a low chain polarity. |
---|---|
ISSN: | 0266-3538 1879-1050 |
DOI: | 10.1016/j.compscitech.2012.08.003 |