-phenylenediamine, in the fixed electrolysis time. The behavior observed during the elimination of 2,4-DNa is due to its difficulty in degrading the chlorine groups in its aromatic ring which makes 2,4-DNa a more stable molecule. In the first oxidation stage, 2,4-dichlorophenol (2,4-DP) is produced in all cases, but on Si/BDD, this intermediate is quickly consumed. From the polarization curves and Tafel analysis, a reaction scheme for the formation and consumption of 2,4-DP was proposed.
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Santos et al. (2020) studied this question.
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