Abstract
Sorption–desorption equilibria of six pyrethroids (permethrin, cyfluthrin, cypermethrin, λ-cyhalothrin, deltamethrin and fenvalerate) and mirex were determined in soils possessing a range of organic content (1.15–2.46%). Solutions (in deionized water, pH 6.5–7.4) of the samples were shaken using a mechanical shaker for 24 h. The suspensions were centrifuged and aliquots of clear supernatant were passed through a C-18 column (SPE extraction). The eluates were concentrated to dryness before a volumetric standard was added. The analytes were determined by gas chromatography with negative ion chemical ionization mass spectrometry (GC/MS-NICI) either in SIR or SCN mode. Sorption isotherm parameters (n and k) were calculated according to the Freundlich equation. The values of n are around unity. Permethrin and cyfluthrin were the least sorbed pyrethroids, k<2, mirex and fenvalerate the most. The effect of the pH on sorption was examined also (at pH values 2, 4, 6 and 9). Sorption behaviour on different soils and silica was also examined. Desorption studies were conducted on the same pyrethroid solutions. After sorption, the supernatant was replaced with a similar volume of deionized water. Desorption was achieved by removing all the supernatant from the centrifuged samples and then replacing it with deionized water. This equilibration process was repeated five times. Each time the suspension was centrifuged, concentrated and analyzed using GC/MS analysis. The residual amount of pyrethroid on the soil was calculated as the difference between the initial amount and the desorbed amount (mass balance).
Notes
aTotal desorption steps (mg L−1).
bSorption (mg L−1).
*Desorption steps (µg L−1).