Ultralow percolation threshold in polyamide 6.6/MWCNT composites

When incorporating multiwalled carbon nanotubes (MWCNTs) synthesised by the aerosol-CVD method using different solvents into polyamide 6.6 (PA66) by melt mixing an ultralow electrical percolation threshold of 0.04. wt.% was found. This very low threshold was assigned to the specific characteristic of the MWCNTs for which a very high aspect ratio, a good dispersability in aqueous surfactant dispersions, and relatively low oxygen content near the surface were measured. The investigation of the composites by transmission electron microscopy on ultrathin cuts as well as by scanning electron microscopy combined with charge contrast imaging on compression moulded plates illustrated a good MWCNT dispersion within the PA66 matrix and that the very high aspect ratio of the nanotubes remained even after melt processing. Additionally, the thermal behaviour of the PA66 composites was investigated using differential scanning calorimetry (DSC) showing that the addition of only 0.05. wt.% MWCNT leads to an increase of the onset crystallization temperature of 11. K

Influence of small scale melt mixing conditions on electrical resistivity of carbon nanotube-polyamide composites

Polyamide 6 (PA6) and polyamide 6.6 (PA66) were filled with multiwalled carbon nanotubes (MWNT) using small scale melt mixing under variation of processing conditions, including temperature, rotation speed, and mixing time. In PA66 an electrical percolation threshold of 1 wt% MWNT was found which is lower than that of PA6 at 2.5-4 wt%. In both cases mixing conditions influenced strongly the dispersion and distribution of CNT and the electrical volume resistivity, whereas crystallisation behaviour was only slightly changed. With increasing mixing energy input remaining agglomerates were less in number and smaller, leading to better dispersion. On the other hand, in samples containing 5 wt% MWNT in PA6 electrical volume resistivity showed a minimum at a quite low energy input and then increased considerably with further input of mixing energy. This increase may be related to MWNT breaking during mixing and encapsulation of MWNT by the polyamide chains. © 2008 Elsevier Ltd. All rights reserved

Multiwalled carbon nanotubes produced by a continuous CVD method and their use in melt mixed composites with polycarbonate

In this study, two samples of multiwalled carbon nanotubes (MWNT) were synthesized by CVD of acetylene over Fe2Co catalysts supported by CaCO3 using different temperatures. The material produced at 660 °C (MWNT600) shows slightly better performance as evidenced by lower mean tube diameter and better conductivity as compared to the sample produced at 700 °C (MWNT700). In addition, it has a higher [O]:[C] ratio. Both materials were incorporated into polycarbonate using melt mixing using a small scale compounder. The results prove that these materials are very suitable for polymer composite applications as they show low electrical percolation concentration and good mechanical enhancement. The percolation threshold is as low as <0.875 wt% for MWNT660 and <1 wt% for MWNT700. MWNT700 showed slightly better dispersability as evidenced from light microscopy, SEM, and TEM. The effects in the stress-strain curves are similar in both composites, indicating a stress increase with MWNT incorporation

Modification with alkyl chains and the influence on thermal and mechanical properties of aromatic hyperbranched polyesters

All-aromatic hyperbranched polyesters with hydroxy endgroups were functionalized with aliphatic n-alkyl carboxylic acids. The length of the n-alkyl chain as well as the degree of modification were varied and the resulting, partially amphiphilic polymers were characterized by differential scanning calorimetry (DSC). With both increasing degree of modification and increasing length of the alkyl chain the glass transition temperature decreases due to reduced intermolecular hydrogen bonding. When the alkyl chains start to crystallize Tg of the hyperbranched polymers increases again. The mechanical properties of the former brittle hyperbranched polyester were improved by modification with C12 chains and a stable free standing film was obtained by compression molding. The film was investigated by means of dynamic mechanic analysis (DMA) and microscopy, exhibiting a low temperature thermal transition and phase separation within the scale of a light microscope. Furthermore melt rheology measurements were performed on the starting polymer and on the C12 modified product. The complex viscosity is reduced strongly by the modification of the aromatic hyperbranched polyester.