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Transformation of polycyclic aromatic hydrocarbons into non-polycyclic derivatives in model aqueous systems.
The fate of polycyclic aromatic hydrocarbons (PAHs) in aqueous systems was studied. The studied PAHs were parent compounds – 3-nitrotoluene and phenanthrene – as well as their fluorine-containing analogs – 2-nitrotoluene, fluorophenanthrene and fluoroanthracene. The experiments were performed in the presence of humic substances. The quantities of transformed PAHs were determined using gas chromatography coupled with mass spectrometry. The results revealed that all studied PAHs were transformed mainly via ring cleavage. This transformation took place exclusively in the aqueous phase, in the presence of humic substances. In the case of the first group of PAHs (non-halogenated nitro-PAHs), this transformation was catalyzed by humic substances. In the case of fluorophenanthrene, both the nitro-PAH and fluorophenanthrene in the presence of humic substances were transformed into the corresponding dinitro-PAHs and fluorophenanthrene oxime, respectively. The first group of studied PAHs (halogenated nitro-PAHs) did not undergo any transformation.Q:

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