Abstract
Molecular iodine was removed from
polypyrrole by electrochemical reduction of slurries at a mercury cathode. This
method was found to be more effective than the treatment of rigid or packed
polymer electrodes.
Voltammetric plots indicated that two
reductions occurred, at potentials insensitive to pH. The current passage was
dependent on the iodine content, while partial reduction or solvent extraction
deleted the first current peak. Complete reduction or alkali treatment removed
both peaks, whereas iodide in solution increased the reduction potentials. From
this evidence it is postulated that the first peak is due to iodine in
solution, the second to iodine present as a charge-transfer complex of
polypyrrole. By estimating the amount of iodine and iodide present in the
electrolyte the reduction potential for dissolved iodine was calculated and
found to agree with that observed for the first peak in the slurry reduction.
Confirmation of this potential was obtained in the reduction of a blank containing
the found amounts of iodine and iodide.
Quantitative data were obtained for the
reduction of slurries in neutral electrolytes. There was reasonable agreement
between coulometric estimations and the iodine removed, after correction for
iodide already present, provided that the anode reaction did not supply
reducible material to the catholyte. Reduction of iodine by polypyrrole itself
did not appear significant in neutral suspensions.
Iodine was readily removed
electrochemically from the early polymers which contained only about 2.2
m-equiv/g. A later polymer contained almost a third more iodine and required
prolonged reduction times which were cut considerably by the use of a silver
anode to mop up iodide ion as it was formed. The reduction products were
compared for changes in acidity, resistivity, and oxygen content. I.
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