ABSTRACT
In the last few years many new reaction routes and intermediates have been discovered in the mechanism of the Belousov-Zhabotinsky (BZ) reaction with the aid of high performance liquid chromatography (HPLC). These previous HPLC studies, however, were limited to the Ce(4+)-organic substrate (malonic or bromomalonic acid) systems only. Very recently some measurements were made on a cerium catalysed full BZ system but only in its induction period. The present work follows the evolution of the main chemical components in a cerium and in a ferroin catalysed full BZ system from the start until the end of the oscillatory regime in a batch reactor. While recording the potential oscillations of a bromide selective electrode we measured from time to time the concentration of the following components: malonic and bromomalonic acids and bromate as main components; malonyl malonate, ethanetetracarboxylic and bromoethenetricarboxylic acids which are recombination products of organic free radicals; oxidized intermediates: tartronic, oxalic (OA) and mesoxalic (MOA) acids, and brominated products: dibromoacetic and tribromoacetic acids. Recombination products are generated in the intervals when the autocatalytic reaction is "switched off". In the course of the autocatalytic periods, however, the organic radicals react with the inorganic bromine dioxide radical mainly which leads to the formation of MOA and OA. Due to a very fast Ce(4+)-MOA reaction, MOA can be detected in the ferroin catalysed BZ system only. Our model calculations deal exclusively with the cerium catalysed system. The suggested new Marburg-Budapest-Missoula (MBM) model includes both negative feedback loops (bromous acid-bromide ion Oregonator type and bromine dioxide-organic free radicals Radicalator type feedback) and the recently discovered radical-radical recombination reactions. Comparison of the experimental data with the model calculations shows a good qualitative agreement but some open problems still remain. To overcome these problems oxygen atom transfer and other redox reactions are proposed.
