New insights into clopyralid degradation by sulfate radical: Pyridine ring cleavage pathways

Abstract

Contamination by herbicides such as clopyralid (CLP) poses a significant threat to human health and ecological systems. In the present study, efficient removal of CLP was achieved by thermo activated persulfate, among which sulfate radical was identified as the predominant oxidizing species responsible for the decontamination. Based on high resolution LC-MS, derivatization method and density functional theory (DFT) computation, the detailed oxidation pathways and mechanisms were proposed. The primary oxidation pathways included dechlorination-hydroxylation, decarboxylation and the formation of quinone-like moieties. Afterwards, numerous intermediate byproducts ranging from high molecular to very small ones were identified, suggesting the pyridine ring was damaged during the thermo activated persulfate process. The detected products containing six and five carbons indicated the pyridine ring cleavage would take place on the quinone-structure intermediate. Further oxidation could continue by breaking each bond on the ring-cleavage product, yielding a series of short-chain carbonyl chemicals, carboxylic acids and inorganic ions. In addition, the presence of dissolved oxygen (DO) was favorable to CLP degradation, indicating DO played an important role in applying such technology. The degradation rate constants of CLP increased appreciably with increasing temperature, and acidic pH facilitated the CLP degradation. The results obtained in this work would increase our understanding on the environmental fates of nitrogen heterocyclic compounds during sulfate radical (SO4•−)-based advanced oxidation processes (SR-AOPs).