The
bromate–phenolsulfonate reaction was found to exhibit
spontaneous oscillations in a batch reactor, where the addition of
small amounts of ferroin would result in nonoscillatory behavior.
As the ferroin concentration was increased, the system produced very
rich nonlinear behavior, including three isolated oscillatory regimes
that were separated by as long as 48 h nonoscillatory period. The
long-lasting nonlinear behavior may be attributed to the slow desulfonation
of phenolsulfonate in an acidic solution, forming phenol-like intermediates.
However, unlike the bromate–phenol oscillator, oxygen was found
to greatly influence the reaction, and various complex oscillations
could be observed by tuning the oxygen concentration. Mechanistic
studies performed through employing 1H NMR spectroscopy
and mass spectrometry to measure intermediate species at different
stages of the reaction were able to identify 1,4-benzoquinone, 2-bromo-1,4-benzoquinone,
2,6-dibromo-1,4-benzoquinone, and 2,4,6-tribromophenol as major components
during the reaction.