JEQ Journal of Natural Resources and Life Sciences Education
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Published in J. Environ. Qual. 33:605-611 (2004).
© ASA, CSSA, SSSA
677 S. Segoe Rd., Madison, WI 53711 USA

TECHNICAL REPORT

Organic Compounds in the Environment

Surface Retention and Photochemical Reactivity of the Diphenylether Herbicide Oxyfluorfen

Laura Scranoa, Sabino A. Bufo*,a, Tommaso R. I. Cataldia and Triantafyllos A. Albanisb

a Dipartimento di Chimica, Università della Basilicata, Via N. Sauro 85, 85100 Potenza, Italy
b Department of Chemistry, University of Ioannina, 45110 Ioannina, Greece

* Corresponding author (bufo{at}unibas.it).

Received for publication January 24, 2003. The photochemical behavior of oxyfluorfen [2-chloro-1-(3-etoxy-4-nitrophenoxy)-4-(trifluoromethyl) benzene] on two Greek soils was investigated. Soils were sampled from Nea Malgara and Preveza regions, characterized by a different organic matter content. Soils were spiked with the diphenyl-ether herbicide and irradiation experiments were performed either in the laboratory with a solar simulator (xenon lamp) or outside, under natural sunlight irradiation; other soil samples were kept in the dark to control the retention reaction. Kinetic parameters of both retention and photochemical reactions were calculated using zero-, first- and second- (Langmuir–Hinshelwood) order equations, and best fit was checked through statistical analysis. The soil behaviors were qualitatively similar but quantitatively different, with the soil sampled from the Nea Malgara region much more sorbent as compared with Preveza soil. All studied reactions followed second-order kinetics and photochemical reactions were influenced by retaining capability of the soils. The contributions of the photochemical processes to the global dissipation rates were also calculated. Two main metabolites were identified as 2-chloro-1-(3-ethoxy-4-hydroxyphenoxy)-4-(trifluoromethyl)benzene and 2-chloro-1-(3-hydroxy-4-nitrophenoxy)-4-(trifluoromethyl)benzene.


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JEQ 2004 33: 413-418. [Full Text]  






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