The electrochemical copolymerization of aniline and N,N,N'-trimethylthionin
(azure B) in aqueous solutions has been carried out using the potential sw
eep method. The optimum conditions for the coelectrodeposition are that the
pH value and the temperature of the electrolytic solution are controlled a
t 5.57 and 30 degreesC, respectively, and the scan potential range is set b
etween -0.25 and 1.10 V (versus SCE). The copolymerization rate of aniline
and azure B is about 3 times larger than that of aniline in the absence of
azure B. The copolymerization of aniline and azure B was verified from the
results of visible spectra during electrolysis, FTIR spectra and the atomic
force microscopy (AFM) images of the polymers. The in situ visible spectru
m for the electrolysis of the solution containing aniline and azure B is di
fferent from that of the respective aniline and azure B. The FTIR spectrum
of the copolymer is not a superposition of that of polyaniline and poly(azu
re B). The AFM image of the copolymer is different from those of polyanilin
e and poly(azure B) and is not a mixture of individual polymers. The conduc
tivity of the copolymer synthesized at pH 5.57 is four orders of magnitude
higher than that of polyaniline synthesized under the same conditions, but
in the absence of azure B. The electrochemical properties of the copolymer
are mainly attributed to polyaniline, but the copolymer has a better electr
ochemical reversibility and a much faster charge transfer than those of pol
yaniline.