Fujiwara Kitao, Ishige Yuko, Inoue Yu-Ichi, Taigo Sunao, Sasaki Takana, Aoki Motohide, Shirasaki Hidekazu, Furuno Masahiro
School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.
J Environ Sci Health A Tox Hazard Subst Environ Eng. 2007 Feb 15;42(3):225-30. doi: 10.1080/10934520601131284.
The solar-induced decomposition of 10 polycyclic aromatic hydrocarbons (PAHs) was observed in aqueous media. All 10 PAHs observed were half-decomposed within 120 min. Among anthracene derivatives, the decomposition rates were: anthracene = 1-methylanthracene < 2-methylanthracene < 9-methylanthracene < 9,10-dimethylanthracene approximately 2-aminoanthracene. The addition of commercial humic acid had no effect on the decomposition rates of these PAHs. Deuterium water also hastened the decomposition of PAH. The products obtained by the solar radiation of PAH after extraction to DCM were mainly ketone and hydroxyl derivatives. To explain these results, reactivities and electron charges at the constituent carbon atoms in each anthracene derivative were examined by an ab initio molecular orbital calculation method.
在水介质中观察到了10种多环芳烃(PAHs)的光致分解。观察到的所有10种PAHs在120分钟内均分解了一半。在蒽衍生物中,分解速率为:蒽 = 1-甲基蒽 < 2-甲基蒽 < 9-甲基蒽 < 9,10-二甲基蒽 ≈ 2-氨基蒽。添加商业腐殖酸对这些PAHs的分解速率没有影响。重水也加速了PAH的分解。PAH经二氯甲烷萃取后进行太阳辐射得到的产物主要是酮和羟基衍生物。为了解释这些结果,通过从头算分子轨道计算方法研究了每种蒽衍生物中组成碳原子的反应性和电子电荷。