Chan K H, Chu W
Department of Civil and Structural Engineering, Research Centre for Environmental Technology and Management, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
Water Res. 2005 May;39(10):2154-66. doi: 10.1016/j.watres.2005.03.029.
The photolytic destruction of Atrazine (ATZ) following a surfactant-aided soil-washing process was investigated in the presence of humic acid (HA). A non-ionic surfactant, Brij 35, was found to be a good solving agent, extracting ATZ without causing any retardation effect on the photolysis process. However, the HA that was co-extracted from the surfactant-aided soil-washing system was found to be capable of improving the photolysis of ATZ at low concentrations, while quenching the photodegradation of ATZ at higher concentrations. By considering the light attenuation effect due to surfactant and HA, the quantum yields of the system with respect to the proposed reaction mechanisms of the associated excited states of ATZ were investigated and modeled. The relative kinetic rates of the dominant reaction mechanisms (i.e., deactivation of triplet, direct photolysis of triplet, product formation, and quenching of triplet) were then compared.
在腐殖酸(HA)存在的情况下,研究了表面活性剂辅助土壤冲洗过程中阿特拉津(ATZ)的光解破坏情况。发现非离子表面活性剂Brij 35是一种良好的溶剂,能够提取ATZ,且对光解过程没有任何阻滞作用。然而,从表面活性剂辅助土壤冲洗系统中共萃取的HA在低浓度时能够促进ATZ的光解,而在高浓度时会抑制ATZ的光降解。考虑到表面活性剂和HA引起的光衰减效应,研究并模拟了该系统相对于ATZ相关激发态的拟议反应机制的量子产率。然后比较了主要反应机制(即三重态失活、三重态直接光解、产物形成和三重态猝灭)的相对动力学速率。