AI Article Synopsis

  • The absorption spectra of five pesticides (2,4-D, cymoxanil, fenpropidin, isoproturon, and pyrimethanil) were measured in aqueous solutions using a CCD detector, finding their molar absorptivity coefficients across a 240-344 nm wavelength range.
  • Significant molar absorptivity values were obtained for each pesticide at 253.7 nm using a Hg-lamp, with 2,4-D at 145, cymoxanil at 7940, fenpropidin at 196, isoproturon at 7330, and pyrimethanil at 13200 (in M(-1) cm(-1)).
  • The study concluded that under sunlight,

Article Abstract

The absorption spectra of five pesticides, namely 2,4-dichloro-phenoxy acetic acid (2,4-D), cymoxanil, fenpropidin, isoproturon and pyrimethanil, have been measured in aqueous solution using a set-up consisting of two parallel absorption cells coupled to a CCD detector. The absolute values of their molar absorptivity coefficients epsilon were determined in the wavelength-range 240-344 nm with a deuterium-lamp at room temperature (298+/-2 K). Using the Beer-Lambert law, values of epsilon were also determined at 253.7 nm with a Hg-Lamp: epsilon = 145+/-14 for 2,4-D, epsilon = 7940+/-920 for cymoxanil, epsilon = 196+/-14 for fenpropidin, epsilon = 7330+/-880 for isoproturon, epsilon = 13200+/-1400 for pyrimethanil (in units of M(-1) cm(-1)). The quoted errors correspond to 2 sigma obtained from the least square fit analysis and the estimated systematic error of 5% due to the uncertainties in aqueous concentrations. For all the studied compounds, the absorbances measured were lower than 2.3 and did not exhibit any deviation from the Beer-Lambert's law. Our experimental data are discussed and compared to UV spectra of similar molecules when such data were available in the literature. Based on their UV spectra and the calculated fractions of these pesticides in the aqueous phase, their direct photolysis under sunlight environment could occur, except may be for fenpropidin, either in water surfaces or in aqueous droplets contained in the atmospheric clouds.

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Source
http://dx.doi.org/10.1016/j.saa.2005.04.040DOI Listing

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