Exposure of polycyclic aromatic hydrocarbons (PAHs) to sunlight results in
rapid structural photomodification generally via oxidation reactions. These
PAH modification products are in many cases more toxic than their parent c
ompounds. In this study, anthracene (ANT), a rapidly photooxidized PAH, was
irradiated with simulated solar radiation (SSR, 100 mu mol m(-2) s(-1)) in
aqueous solution to examine the photomodification pathway. The photoproduc
ts formed were identified by HPLC. The ANT product profile after 9 h in SSR
was very complex, with more than 20 compounds detected. The photoproducts
formed were anthraquinones, benzoic acids, benzaldehydes and phenols showin
g the process to be oxidative in nature. Some of the anthraquinones were th
emselves subject to photooxidation, and were thus intermediates in the prod
uct pathway. The kinetics of ANT photooxidation revealed a pseudo first-ord
er reaction with a half-life of 2 h under the SSR source used. The kinetics
of product formation allowed deduct-ion of a probable photomodification pa
thway. This study indicates that PAH photooxidation products are likely to
exist as complex, dynamically changing mixtures in PAH contaminated aquatic
environments. (C) 2000 Elsevier Science Ltd. All rights reserved.