芘
环境化学
沉积物
多环芳烃
化学
污染
碳氢化合物
持久性有机污染物
分配系数
环境科学
污染
水污染
萘
色谱法
生态学
地质学
有机化学
古生物学
生物
作者
Steven B. Hawthorne,Carol B. Grabanski,David J. Miller
摘要
Abstract Polycyclic aromatic hydrocarbon (PAH) partitioning coefficients between sediment organic carbon and water ( K OC ) values were determined using 114 historically contaminated and background sediments collected from eight different rural and urban waterways in the northeastern United States. More than 2,100 individual K C values were measured in quadruplicate for PAHs ranging from two to six rings, along with the first reported K OC values for alkyl PAHs included in the U.S. Environmental Protection Agency's (U.S. EPA) sediment narcosis model for the prediction of PAH toxicity to benthic organisms. Sediment PAH concentrations ranged from 0.2 to 8,600 μg/g (U.S. EPA 16 parent PAHs), but no observable trends in K OC values with concentration were observed for any of the individual PAHs. Literature K OC values that are commonly used for environmental modeling are similar to the lowest measured values for a particular PAH, with actual measured values typically ranging up to two orders of magnitude higher for both background and contaminated sediments. For example, the median log K OC values we determined for naphthalene, pyrene, and benzo[ a ]pyrene were 4.3, 5.8, and 6.7, respectively, compared to typical literature K OC values for the same PAHs of 2.9, 4.8, and 5.8, respectively. Our results clearly demonstrate that the common practice of using PAH K OC values derived from spiked sediments and modeled values based on n ‐octanol–water coefficients can greatly overestimate the actual partitioning of PAHs into water from field sediments.
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