Reactivity of Cyanobacteria Metabolites with Ozone: Multicompound Competition Kinetics.
Valentin RougéUrs von GuntenElisabeth M L JanssenPublished in: Environmental science & technology (2024)
Cyanobacterial blooms occur at increasing frequency and intensity, notably in freshwater. This leads to the introduction of complex mixtures of their products, i.e., cyano-metabolites, to drinking water treatment plants. To assess the fate of cyano-metabolite mixtures during ozonation, a novel multicompound ozone (O 3 ) competition kinetics method was developed. Sixteen competitors with known second-order rate constants for their reaction with O 3 ranging between 1 and 10 8 M -1 s -1 were applied to cover a wide range of the O 3 reactivity. The apparent second-order rate constants ( k app,O3 ) at pH 7 were simultaneously determined for 31 cyano-metabolites. k app,O3 for olefin- and phenol-containing cyano-metabolites were consistent with their expected reactivity (0.4-1.7 × 10 6 M -1 s -1 ) while k app,O3 for tryptophan- and thioether-containing cyano-metabolites were significantly higher than expected (3.4-7.3 × 10 7 M -1 s -1 ). Cyano-metabolites containing these moieties are predicted to be well abated during ozonation. For cyano-metabolites containing heterocycles, k app,O3 varied from <10 2 to 5.0 × 10 3 M -1 s -1 , giving first insights into the O 3 reactivity of this class of compounds. Due to lower O 3 reactivities, heterocycle- and aliphatic amine-containing cyano-metabolites may be only partially degraded by a direct O 3 reaction near circumneutral pH. Hydroxyl radicals, which are formed during ozonation, may be more important for their abatement. This novel multicompound kinetic method allows a high-throughput screening of ozonation kinetics.