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Updated: Jan 14, 2026

Separation of Aldehydes and Reactive Ketones from Mixtures Using a Bisulfite Extraction Protocol
Published on: April 2, 2018
Reaction kinetics of organic sulfur compounds with ozone in aqueous phase
Simon A Rath1, Maria Lia Halder2, Urs von Gunten1
1Eawag, Swiss Federal Institute of Aquatic Science and Technology, CH-8600 Dübendorf, Switzerland; School of Architecture, Civil and Environmental Engineering (ENAC), Ecole Polytechnique Fédérale Lausanne (EPFL), CH-1015 Lausanne, Switzerland.
Abstract:
Sulfur functional groups are abundant in natural organic compounds, pesticides and pharmaceuticals. Kinetic data of their aqueous reaction with ozone is only available for a very small set of compounds and sometimes contradictory, making predictions on their fate during ozonation processes difficult. Therefore, second-order rate constants kO₃ were determined for 37 sulfur-containing compounds and trends in reactivity were identified. For the determination of kO₃ via competition kinetics, aldicarb was established as pH-independent competitor (kO₃=1.0×10⁶ M⁻¹s⁻¹). Sulfides (thioethers) react very fast with ozone (kO₃≈2×10⁶ M⁻¹s⁻¹). Exceptions are sulfides, which are π-conjugated to electron-withdrawing groups (e.g., thiocarbamates, kO₃≈10⁰-10³ M⁻¹s⁻¹), and β-lactam antibiotics (kO₃≈10³ M⁻¹s⁻¹), which are deactivated to different degrees. Thiols exhibit pH-dependent reactivities, though the dependency is much smaller than previously reported, ranging from kO₃+SH≈104 M⁻¹s⁻¹ to kO₃+S⁻≈10⁶ M⁻¹s⁻¹, but an unprecedented pH-dependency is observed. A deactivating effect of neighboring groups renders the reactivity of the disulfide cystine and similar compounds pH-dependent (kO₃(pH3)≈10² M⁻¹s⁻¹, kO₃(pH7)≈10⁵ M⁻¹s⁻¹) while disulfides without acidic functional groups exhibit pH-independent reactivities (kO₃≈2×10⁵ M⁻¹s⁻¹). Further oxidized functional groups like sulfoxides or thiosulfinate esters are unreactive (kO₃≈10⁰-10¹ M⁻¹s⁻¹), but sulfinates are very susceptible to ozonation (kO₃≈2×10⁶ M⁻¹s⁻¹). A definitive explanation for this difference is still lacking. For non-N-alkylated isothiazolones, an unexpected pH-dependency is observed, similar to cysteines. The reactivity at pH 7 differs by 4 orders of magnitude, whether or not N-alkylated (kO₃≈10² M⁻¹s⁻¹, kO₃≈10⁶ M⁻¹s⁻¹, respectively). Overall, the data presented provides novel insights into the ozone reactivity of sulfur compounds as a basis for a better assessment of their fate during ozonation.
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