Acetaminophen Degradation By Hydroxyl And Organic Radicals In The Peracetic Acid-Based Advanced Oxidation Processes: Theoretical Calculation And Toxicity Assessment

The research on the mechanisms and kinetics of radical oxidation in peracetic acid-based advanced oxidation processes was relatively limited. In this work, HO' and organic radicals mediated reactions of acetaminophen (ACT) were investigated, and the reactivities of important organic radicals (CH3COO' and CH3COOO') were calculated. The results showed that initiated reaction rate constants of ACT are in the order: CH3COO' (5.44 x 1010 M-1 s- 1) > HO' (7.07 x 109 M-1 s- 1) > CH3O' (1.57 x 107 M-1 s- 1) > CH3COOO' (3.65 x 105 M-1 s- 1) >> 'CH3 (5.17 x 102 M-1 s- 1) > CH3C'O (1.17 x 102 M-1 s- 1) > CH3OO' (11.80 M-1 s-1). HO', CH3COO' and CH3COOO' play important roles in ACT degradation. CH3COO' is another important radical in the hydroxylation of aromatic compounds in addition to HO'. Reaction rate constants of CH3COO' and aromatic compounds are 1.40 x 106 - 6.25 x 1010 M-1 s-1 with addition as the dominant pathway. CH3COOO' has high reactivity to phenolate and aniline only among the studied aromatic compounds, and it was more selective than CH3COO'. CH3COO'-mediated hydroxylation of aromatic compounds could produce their hydroxylated products with higher toxicity.