Phototransformation of Propiconazole In Aqueous Media

The photolysis of propiconazole in pure water, in water containing humic substances, and in natural water was investigated. The reaction rates were determined, and the main photoproducts were identified with the help of HPLC−mass spectrometry and by NMR. The quantum yield for direct photolysis was 0...

Full description

Saved in:
Bibliographic Details
Published inJournal of agricultural and food chemistry Vol. 49; no. 11; pp. 5377 - 5382
Main Authors Vialaton, Delphine, Pilichowski, Jean-François, Baglio, Daniela, Paya-Perez, Ana, Larsen, Bo, Richard, Claire
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 01.11.2001
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The photolysis of propiconazole in pure water, in water containing humic substances, and in natural water was investigated. The reaction rates were determined, and the main photoproducts were identified with the help of HPLC−mass spectrometry and by NMR. The quantum yield for direct photolysis was 0.11 ± 0.01 at the maximum of absorption (269 nm). Photocyclization after HCl elimination and photohydrolysis of the cyclized intermediate were the main reaction pathways at 254 nm. By contrast, oxidation prevailed over dechlorination in simulated or natural solar light. Humic substances (10 mg·L-1) and naturally occurring chromophores contained in natural water enhanced the rate of propiconazole photodegradation in solar light. Half-life in June in Clermont-Ferrand (latitude 46°N) was found to be 85 ± 10 h in pure water and 60 ± 10 h in natural water; showing that photodegradation of propiconazole in natural waters involves both direct photolysis and photoinduced reactions. Keywords: Propiconazole; direct photolysis; photoinduced transformation; humic substances; natural water; solar light
Bibliography:istex:F7BDBED1EBCFC5E8D9F140550F80C92E1B3570F2
ark:/67375/TPS-3VGHTWS9-Z
ISSN:0021-8561
1520-5118
DOI:10.1021/jf010253r