Kinetics and hydrolysis of fenamiphos, fipronil, and trifluralin in aqueous buffer solutions

Citation
A. Ramesh et M. Balasubramanian, Kinetics and hydrolysis of fenamiphos, fipronil, and trifluralin in aqueous buffer solutions, J AGR FOOD, 47(8), 1999, pp. 3367-3371
Citations number
22
Categorie Soggetti
Agricultural Chemistry","Chemistry & Analysis
Journal title
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
ISSN journal
00218561 → ACNP
Volume
47
Issue
8
Year of publication
1999
Pages
3367 - 3371
Database
ISI
SICI code
0021-8561(199908)47:8<3367:KAHOFF>2.0.ZU;2-G
Abstract
Hydrolyses of fenamiphos, fipronil, and trifluralin were studied in aqueous buffer solutions of pH 4.1, 7.1, and 9.1 at different temperatures, 5, 22 +/- 1, 32 +/- 1, and 50 +/- 1 degrees C. Fenamiphos, fipronil, and triflura lin were found to be more stable in acidic and neutral buffer solutions at temperatures of 5 and 22 +/- 1, and dissipation is rapid at 50 +/- 1 degree s C. In basic buffer and at higher temperature, degradation of fenamiphos w as found to be very rapid when compared with fipronil and trifluralin. The rate constants calculated at 32 degrees C for fenamiphos were 2349.4 x 10(- 8) (pH 4.1), 225.2 x 10(-8) (pH 7.1), and 30476.0 x 10(-8) (pH 9.1); for fi pronil 1750.0 x 10(-8) (pH 4.1), 3103.0 x 10(-8) (pH 7.1), and 3883.0 x 10( -8) (pH 9.1); and for trifluralin 2331.0 x 10(-8) (pH 4.1), 2360.0 x 10(-8) (pH 7.1), and 3188.0 x 10(-8) (pH 9.1). On the basis of rate constant valu es, these pesticides appeared to be more susceptible to hydrolysis than syn thetic organophosphorus compounds such as chlorpyriphos, diazinon, malathio n, and ronnel. DT50 values calculated at 32 degrees C were 228 (pH 4.1), 53 10.24 (pH 7.1), and 37.68 (pH 9.1) h for fenamiphos; 608.6 (pH 4.1), 373.9 (pH 7.1), and 270.2 (pH 9.1)h for fipronil; and 502.1 (pH 4.1), 496.8 (pH 7 .1), and 355.7 (pH 9.1) h for trifluralin.