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The carbonization of colloidal polyaniline nanoparticles to nitrogen-containing carbon analogues
The carbonization of nanostructures afforded by conducting polymers represents a new route to the preparation of functional nanostructured carbons. The exposure of colloidal polyaniline particles stabilized with poly(N‐vinylpyrrolidone) or silica nanoparticles at 650 °C in inert atmosphere led, in b...
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Published in: | Polymer international 2010-07, Vol.59 (7), p.875-878 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The carbonization of nanostructures afforded by conducting polymers represents a new route to the preparation of functional nanostructured carbons. The exposure of colloidal polyaniline particles stabilized with poly(N‐vinylpyrrolidone) or silica nanoparticles at 650 °C in inert atmosphere led, in both cases, to nitrogen‐containing carbonaceous materials with specific surface areas of 200 and 205 m2 g−1, respectively, and conductivities of 8.3 × 10−7 and 1.9 × 10−10 S cm−1, respectively. The latter material contained 77 wt% of silica. The original particulate nanostructure of the samples was preserved after carbonization. The carbon‐to‐nitrogen atomic ratio was 7.2 and 7.9; the nitrogen content in the carbonized polyaniline–poly(N‐vinylpyrrolidone) particles was 10.8 wt%. Thermogravimetric analysis in air revealed their stability to be up to 500 °C. This is comparable with commercial multi‐wall carbon nanotubes, which have similar areas of application. The nitrogen‐containing carbons are potentially useful as supports for catalysts and in applications where carbon of higher hydrophilicity would be of benefit. Copyright © 2010 Society of Chemical Industry
The carbonization of colloidal polyaniline nanoparticles stabilized with poly(N‐vinylpyrrolidone) or silica leads to nitrogen‐containing carbons having large surface areas. The original particulate nanostructure is preserved after carbonization |
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ISSN: | 0959-8103 1097-0126 1097-0126 |
DOI: | 10.1002/pi.2858 |