Properties of nanometal-polyaniline composites
Date
2011-07-21
Authors
Kabomo, Tlhabologo Moses
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Abstract
Polymeric nanocomposites are intimate combinations of a polymer with inorganic
nanoparticles. Such nanomaterials have attracted significant attention over the years
because of their potential uses as chemical sensors, electronic and optical devices, and
as catalysts. For catalytic applications, in particular, small and well dispersed
nanoparticles are desired. We report here the synthesis of gold-polyaniline (AuPANI)
nanocomposites and their catalytic performance. The simple synthetic route involved
pre-organizing the gold ions in polyaniline (PANI) through complexation followed by
the addition of a reducing agent. Control over the degree of reduction of
tetrachloroaurate ions (AuCl4
–) depends on the electrochemical potential of the system
which in turn depends on the molar ratio of the nitrogen atoms on PANI to AuCl4
–.
Gold nanoparticles formed when the AuPANI complexes were reduced with sodium
borohydride and the size of the nanoparticles could be varied with adjustment of the
amount of sodium borohydride used. Low amounts of sodium borohydride induced
slow nucleation rate and were associated with relatively large metallic particles. The
smallest gold nanoparticles with a narrow size distribution were obtained when a ratio
of sodium borohydride:gold of about 6:1 was used. Simple electrolytes like NaCl and
NaOH did not induce the aggregation of Au nanoparticles as predicted by the DLVO
theory. However, chain-like aggregates formed when aggregation was induced by the
reduction of PANI while close-packed aggregates formed when PANI was oxidized
or protonated. The Au nanoparticles were found to be more stable when dispersed on
ring-substibuted PANI than on unsubstituted PANI. The catalytic performance of
AuPANI was evaluated using the reduction of 4-nitrophenol by sodium borohydride.
The reaction was observed to follow the Langmuir-Hinshelwood kinetics.