A method of sample preparation based on use of rotating disk sorptive extraction (RDSE) has been developed for determination of triclosan (TCS) and methyl-triclosan (MTCS) in water samples. The sorptive and desorptive behavior of the analytes was studied by use of a rotating disk coated with polydimethylsiloxane (PDMS) on one of its surfaces. Chemical and extraction behavior were studied to establish the best conditions for extraction. The optimum conditions for both analytes were: sample volume 25 mL, pH 4.5, NaCl concentration 6% (w/v), disk rotational velocity 1,250 rpm, and extraction time 80 min. A desorption time of 30 min was used with 5 mL methanol. The detection limits for TCS and MTCS were 46 and 34 ng L(-1), respectively. Recovery was evaluated at two concentrations, 160 and 800 ng L(-1), and the values obtained were between 80 and 100%. The method was applied to analysis of influent water at two treatment plants in Santiago, Chile.
The extraction device used in rotating-disk sorptive extraction consists of a Teflon disk in which a sorptive phase is fixed on one of its surfaces. Depending on the configuration, the rotation axis of the disk device can be either perpendicular or parallel to its radius, giving rise to two different mass transfer patterns when rotating-disk sorptive extraction is applied in liquid samples. In the perpendicular case (configuration 1), which is the typical configuration, the disk contains an embedded miniature stir bar that allows the disk rotation to be driven using a common laboratory magnetic stirrer. In the parallel case (configuration 2), the disk is driven by a rotary rod connected to an electric stirrer. In this study, triclosan and its degradation product methyl triclosan were used as analyte models to demonstrate the significant effect of the rotation configuration of the disk on the efficiency of analyte mass transfer from water to a sorptive phase of polydimethylsiloxane. Under the same experimental conditions and at a rotation velocity of 1,250 rpm, extraction equilibrium was reached at 80 min when the disk was rotated in configuration 1 and at 30 min when the disk was rotated in configuration 2. The extraction equilibration time decreased to 14 min when the rotation velocity was increased to 2,000 rpm in configuration 2. Because the rotation pattern affects the mass transfer efficiency, each rotation configuration was characterized through the Reynolds number; Re values of 6,875 and 16,361 were achieved with configurations 1 and 2, respectively, at 1,250 rpm.
The bioavailability of polychlorinated biphenyls (PCBs) in soils amended with biosolids was estimated using an aqueous leaching process of the compounds combined with rotating disk sorptive extraction (RDSE), and compared with bioavailability determined through of PCB absorption in wheat plants growing in the same soil-biosolid matrix. The matrices consisted of soil amended with biosolids at doses of 30, 90, and 200 Mg/ha, which increase concomitantly the organic matter content of the matrix. Considering that PCBs were natively absent in both the biosolids and soil used, the compounds were spiked in the biosolids and aged for 10 days. For each biosolid dose, the aqueous leaching profile was studied and equilibrium time was calculated to be 33 h. The leaching fractions determined by RDSE, considering total PCBs studied, were 12, 7, and 6% and the bioavailable fractions absorbed by the wheat root were found to be 0.5, 0.3, and 0.2% for 30, 90, and 200 Mg/ha doses, respectively. Both fractions leachable and bioavailable decrease with both increasing hydrophobicity of the compound (Kow) and increasing in the biosolid dose. It was found that both fractions (leaching and bioavailable) correlated according to the bivariate least squares regression, represented by a coefficient of correlation of 0.86. Therefore, the application of the chemical method involving a leaching procedure is an alternative to estimate the bioavailable fraction of PCBs in wheat plants in a simpler and in a shorter time.
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