Experimental verification of a model describing solid phase microextraction (SPME) of freely dissolved organic pollutants in sediment porewater

To verify a theoretical mass balance and multiple compartment partitioning model developed to predict freely dissolved concentrations (FDCs) of hydrophobic organic chemicals (HOCs) using negligible depletion-solid phase microextraction (nd-SPME), a series of sediment slurry experiments were performe...

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Published inChemosphere (Oxford) Vol. 72; no. 10; pp. 1435 - 1440
Main Authors Yang, Ze-Yu, Maruya, Keith A., Greenstein, Darrin, Tsukada, David, Zeng, Eddy Y.
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.08.2008
Elsevier
Subjects
DDE
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Summary:To verify a theoretical mass balance and multiple compartment partitioning model developed to predict freely dissolved concentrations (FDCs) of hydrophobic organic chemicals (HOCs) using negligible depletion-solid phase microextraction (nd-SPME), a series of sediment slurry experiments were performed using disposable poly(dimethyl)siloxane (PDMS) coated-SPME fibers and 14C-radiolabeled HOC analogs. First, pre-calibration of disposable PDMS coated fibers for four model compounds (phenanthrene, PCB 52, PCB 153 and p,p′-DDE) with good precision (⩽10%) was achieved. Second, sediment slurries spiked and aged with the radiolabeled analogs were extracted by SPME with manipulation of the sediment slurry mass (ms) or the PDMS coating volume (Vf). The measured extent of depletion by SPME (xe) decreased with increasing sediment mass (ms); conversely, xe increased with increasing Vf, which is consistent with the theoretical prediction from our previous model [Yang, Z.-Y., Zeng, E.Y., Maruya, K.A., Mai, B.-X., Ran, Y., 2007b. Predicting organic contaminant concentrations in sediment porewater using solid-phase microextraction. Chemosphere 66, 1408–1414]. Moreover, the SPME-measured FDCs (Cpw,SPME) followed the order of phenanthrene>PCB 52>PCB 153, and the measured and predicted Cpw values were not substantially different from empirically determined values except for p,p′-DDE.
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ISSN:0045-6535
1879-1298
DOI:10.1016/j.chemosphere.2008.05.028