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Thermal and Electrical Properties of Polymer / Multi-Walled<br />
Carbon Nanotubes Nanocomposites<br />
E. Logakis 1* , Ch. Pandis 1 , P. Pissis 1 , J. Pionteck 2 , P. Pötschke 2 , M. Mičušík 3 and M. Omastová 3<br />
1 National Technical University of Athens, Zografou Campus, 15780, Athens, Greece<br />
2 Leibniz Institute of Polymer Research Dresden, 01069 Dresden, Germany<br />
3 Polymer Institute, Slovak Academy of Sciences, 842 36 Bratislava, Slovakia<br />
*E-mail: logmanos@central.ntua.gr<br />
Tel.: (+30) 210 772 2974, Fax: (+30) 210 772 2932<br />
Carbon nanotubes (CNTs) have attracted special interest as new materials for mixing with polymers due to their<br />
exceptional electrical, mechanical and thermal properties. Polymer/CNTs nanocomposites are promising materials with<br />
potential applications as electromagnetic shielding coatings, electrostatically dissipative materials, aerospace structural<br />
materials and active elements in sensors.<br />
Several processing methods are available for the production of polymer / CNT composites. Melt-mixing of CNT into<br />
thermoplastic polymers using conventional processing techniques are particularly desirable, because of the speed, simplicity,<br />
and availability in the plastic industry. This method is also beneficial because is free of solvents and contaminants, which are<br />
present in solution processing methods and in-situ polymerization.<br />
In the present study, the nanocomposites were prepared by melt mixing a starting masterbatch (Hyperion Catalysis, USA)<br />
of polyamide 6 (PA6) or polypropylene (PP) containing 20 wt% multi-walled carbon nanotubes (MWCNTs) with the pure<br />
polymers in a Plasti-corder kneading machine PLE 331 (Brabender, Germany), followed by compression moulding using a<br />
laboratory hydraulic press SRA 100 in order to obtain different concentrations in CNTs.<br />
The purpose of this work is to examine the thermal, electrical and dielectric properties of multi-walled carbon nanotubes<br />
(MWCNT) filled PA6 or PP nanocomposites formed by melt-mixing. To that aim differential scanning calorimetry and<br />
dielectric relaxation spectroscopy were employed. The influence of CNT on the thermal transitions (glass transition<br />
temperature, melting, crystallization) of the pure polymers is investigated. The results are discussed in terms of nucleating<br />
action of CNT and interfacial polymer-filler interactions. Special attention is paid to percolation aspects by both ac and dc<br />
conductivity measurements for the samples which are above the percolation threshold (p c ). Percolation threshold is the<br />
critical concentration of the filler where conducting pathways are formed by CNT and consequently a transition from the<br />
insulating to the conducting phase is observed. p c is usually determined through dc conductivity measurements. In this work<br />
ac measurements were performed, as apart from the determination of dc conductivity, the opportunity to study in detail the<br />
frequency dependence of conductivity is provided by defining the critical frequency (f c ), where the transition from dc to ac<br />
conductivity is observed. Furthermore, the actual aspect ratio (length-to-diameter ratio) of the inclusions in the<br />
nanocomposites is calculated using two different theoretical models (E. J. Garboczi et al. and I. Balberg et al. model) and the<br />
exported values are correlated with the percolation threshold values. It is already known that CNT have the tendency to form<br />
bundles due to van der Waals interactions and the final aspect ratio of CNT in the nanocomposites is much lower, comparing<br />
with the value of an individual nanotube. This fact leads to increased p c values. Besides, the conductivity mechanism is<br />
examined through the temperature dependence of conductivity. Finally, the influence of CNT on the study of dielectric<br />
relaxation mechanisms of PA6 is investigated, to look for effects of CNT on molecular mobility of the polymer matrix, which<br />
may arise from polymer-filler interactions.<br />
Acknowledgement<br />
"This work has been funded by the project PENED 2003. The project is cofinanced 75% of public expenditure through EC -<br />
European Social Fund, 25% of public expenditure through Ministry of Development - General Secretariat of Research and<br />
Technology and through private sector, under measure 8.3 of OPERATIONAL PROGRAMME "COMPETITIVENESS" in<br />
the 3rd Community Support Programme."<br />
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