Measured partition coefficients for parent and alkyl polycyclic aromatic hydrocarbons in 114 historically contaminated sediments: Part 2. Testing the KOCKBC two carbon–type model

Authors

  • Steven B. Hawthorne,

    Corresponding author
    1. Energy & Environmental Research Center, University of North Dakota, Box 9018, Grand Forks, North Dakota 58202, USA
    Current affiliation:
    1. Any opinions, findings, conclusions, or recommendations expressed herein are those of the authors and do not necessarily reflect the views of the sponsors.; Published on the Web 7/23/2007
    • Energy & Environmental Research Center, University of North Dakota, Box 9018, Grand Forks, North Dakota 58202, USA
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  • Carol B. Grabanski,

    1. Energy & Environmental Research Center, University of North Dakota, Box 9018, Grand Forks, North Dakota 58202, USA
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  • David J. Miller

    1. Energy & Environmental Research Center, University of North Dakota, Box 9018, Grand Forks, North Dakota 58202, USA
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Abstract

Polycyclic aromatic hydrocarbon (PAH) desorption partition coefficients between black carbon and water (KBC) were determined using 114 historically contaminated and background sediments from eight different rural and urban waterways. Black carbon was measured after oxidation at 375°C for 24 h. Organic carbon–water partition coefficients (KOC) required for the calculation of KBC values were determined for two- to six-ring parent and C1- to C4-alkyl PAHs based on the lower range of measured KOC values from the same sediments and comparisons to literature KOC values. Approximately 2,050 log KBC values were determined on sediments having a range of total organic carbon from 0.3 to 42% by weight, black carbon from 0.1 to 40% by weight, and total PAH concentrations (U.S. Environmental Protection Agency 16 parent PAHs) from 0.2 to 8,600 μg/g. Contrary to expectations, PAH partitioning was not better explained using the combined KOC and KBC models rather than the simple KOC model (i.e., KBC values for each individual PAH ranged nearly three orders of magnitude). No effect of PAH concentration on measured KBC values was apparent. Values of KBC also showed no trends with total organic carbon, black carbon, or the presence or absence of a nonaqueous phase liquid. Multiple linear regression analysis with KOC and KBC as fitted values also failed to explain the variance of the experimental data (r2 values typically less than 0.20, and standard errors greater than two orders of magnitude). These results demonstrate that models of PAH partitioning that account for different carbon types, although useful for understanding partitioning mechanisms, cannot yet be used to accurately predict PAH partitioning from historically contaminated sediments.

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