4.7 Article

Effect of acid treated multi-walled carbon nanotubes on the mechanical, permeability, thermal properties and thermo-oxidative stability of isotactic polypropylene

Journal

POLYMER DEGRADATION AND STABILITY
Volume 93, Issue 5, Pages 952-967

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymdegradstab.2008.01.033

Keywords

nanocomposites; polypropylene; multi-walled carbon nanotubes; thermal stability; thermo-oxidative stability; gas permeability

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The effect of acid treatment of multi-walled carbon nanotubes (MWCNTs) on the mechanical, thermal and mainly thermo-oxidative stability of isotactic polypropylene (iPP) was evaluated. From the acid treatment surface carboxylic groups were mainly formed, while the nanotubes' length was gradually reduced by increasing the treatment time. Young's modulus, tensile strength and storage modulus of the iPP/MWCNT nanocomposites were increased by increasing the treatment time of the MWCNTs, due to finer dispersion inside the polymer matrix, as revealed by TEM and micro-Raman spectroscopy. Furthermore, the nanotubes acted as nucleating agents, an effect more pronounced with finer filler dispersion. Thermal stability in an inert atmosphere also increased. Thermo-oxidative stability tests in air and O-2 revealed that oxidative degradation took place in two stages. In the first stage, corresponding to temperatures up to 230 degrees C, the MWCNTs accelerated the oxidation of W, while at higher than 300 degrees C temperatures the trend was reversed. Incubation studies proved that, at the first stages, oxidation was due to random chain scission of iPP and oxygen uptake. This behaviour was accelerated by the MWCNTs' surface carboxylic groups and, as found by O-2 permeability studies, was mainly a surface process. In the second stage, due to the shielding effect of MWCNTs, the removal of the gases produced during decomposition was hindered. At this stage the presence of MWCNTs resulted in more thermo-oxidatively stable nanocomposites. (C) 2008 Elsevier Ltd. All rights reserved.

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