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The simultaneous degradation of prochloraz and tebuconazole in water with identification of the main degradation products using liquid chromatography-tandem mass spectrometry.

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Mahmoud M. Awwad, Mahmoud M. Awwad, Mahmoud M. Awwad, Mahmoud M. Awwad, Sherif M. Taha, Sherif M. Taha, Mostafa M.H. Khalil, Mostafa M.H. Khalil, Abdelnaby Mohamed Salem, Mostafa M.H. Khalil, Abdelnaby Mohamed Salem, Abdelnaby Mohamed Salem, Abdelnaby Mohamed Salem, Jean-Marc Chovelonc, Jean-Marc Chovelonc

Summary

Researchers investigated the simultaneous degradation of the fungicides prochloraz and tebuconazole in water, identifying the main breakdown products using liquid chromatography-tandem mass spectrometry. The study demonstrated complete degradation of both compounds under the tested conditions and characterized the resulting metabolite pathways, informing risk assessment for fungicide co-contamination in water systems.

Abstract Prochloraz and tebuconazole are well-known fungicides for broad-spectrum applications, including; medical, industrial, and agricultural. These fungicides are frequently used simultaneously for the protection of various agricultural products. The presence of these fungicides in water doesn't only affect the health of direct consumers but also limits their reuse. In this study, complete degradation of these fungicides and their degradation products were accomplished using thermal-activated persulfate. It takes only 30 min to degrade 97% and 98% of PCZ and TBZ, respectively, in their single presence in water using 1.4 mM persulfate and a temperature of 50 ºC. However, in their simultaneous presence in water, a treatment for a complete one hour is required to degrade 99% and 94% for PCZ and TBZ, respectively, at the same degradation conditions. The persulfate degradation of prochloraz was conducted by the cleavage of the imidazole ring and the subsequent formation of a trichlorophenol. While, persulfate degradation of tebuconazole was mainly accomplished by the formation of a hydroxyl structure, cleavage of the tert-butyl chain, and the subsequent formation of a di-ketone degradation product. The identification of PCZ and TBZ degradation products was determined using the liquid chromatography-tandem mass spectrometry technique (LC-MS/MS) at both positive and negative modes. The suggested structures of these degradation products and their dissipation were confirmed and monitored, respectively, using efficiently developed LC-MS/MS multiple reaction monitoring methods.

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