Cai Zhengqing, Liu Wen, Fu Jie, O'Reilly S E, Zhao Dongye
Environmental Engineering Program, 238 Harbert Engineering Center, Auburn University, Auburn, AL 36849, USA.
Bureau of Ocean Energy Management, GOM Region, Office of Environment, New Orleans, LA 70123, USA.
Environ Pollut. 2017 Oct;229:272-280. doi: 10.1016/j.envpol.2017.05.084. Epub 2017 Jun 7.
This study investigated effects of three model oil dispersants on photodegradation of two model PAHs (anthracene and 9,10-dimethyanthracene (9,10-DMA)) under simulated sunlight. All three dispersants, i.e. Corexit EC9500A, Corexit EC9527A and SPC 1000, promoted the photolysis rate of 9,10-DMA, following the order of Corexit EC9500A > Corexit EC9527A > SPC 1000. The photodegradation rate was well interpreted by a two-stage, first-order kinetic law with a faster initial photolysis rate in the presence of the dispersants. Span 80, Tween 85 and kerosene were found as the key dispersant components, of which Span 80 and Tween 85 promoted the photodegradation by boosting absorbance of solar irradiation while kerosene by dispersing more PAHs in the upper layer of the water column. Dissolved oxygen (DO) inhibited photolysis of anthracene regardless of dispersant resulting from quenching the excited states of the PAH, while DO facilitated photolysis of 9,10-DMA due to the formation singlet oxygen (O) radicals in the presence of oil dispersants. The other ROS, i.e. •O and •OH, played a negligible role on the photodegradation of anthracene and 9,10-DMA. Fluorescence analysis showed that more anthracene was associated with dispersant than 9,10-DMA, which favored the direct transfer of energy to anthracene, while energy is more likely transferred to oxygen to form O in the case of 9,10-DMA. Direct photolysis dominated the photodegradation of anthracene and 9,10-DMA. Both direct ionization of anthracene and the electron transfer from excited 9,10-DMA to oxygen can lead to formation of the corresponding PAH radical cations. Overall, the oil dispersants accelerated the photolysis rates of the PAHs without altering the degradation pathway. The findings are useful for understanding photochemical weathering of dispersed oil components in the environment.
本研究调查了三种模型油分散剂在模拟阳光下对两种模型多环芳烃(蒽和9,10 - 二甲基蒽(9,10 - DMA))光降解的影响。所有三种分散剂,即Corexit EC9500A、Corexit EC9527A和SPC 1000,均促进了9,10 - DMA的光解速率,其顺序为Corexit EC9500A > Corexit EC9527A > SPC 1000。光降解速率可用两阶段一级动力学定律很好地解释,在存在分散剂的情况下初始光解速率更快。发现Span 80、吐温85和煤油是关键的分散剂成分,其中Span 80和吐温85通过提高太阳辐射的吸光度促进光降解,而煤油则通过在水柱上层分散更多的多环芳烃来促进光降解。溶解氧(DO)抑制蒽的光解,无论分散剂如何,这是由于猝灭了多环芳烃的激发态,而在存在油分散剂的情况下,DO由于形成单线态氧(O)自由基而促进9,10 - DMA的光解。其他活性氧,即•O和•OH,在蒽和9,10 - DMA的光降解中作用可忽略不计。荧光分析表明,与9,10 - DMA相比,更多的蒽与分散剂结合,这有利于能量直接转移到蒽上,而在9,10 - DMA的情况下,能量更有可能转移到氧上形成O。直接光解主导了蒽和9,10 - DMA的光降解。蒽的直接电离以及从激发态的9,10 - DMA到氧 的电子转移都可导致相应的多环芳烃自由基阳离子的形成。总体而言,油分散剂加速了多环芳烃的光解速率,而没有改变降解途径。这些发现有助于理解环境中分散油成分的光化学风化。