Cranfield Water Science Institute, Department of Environmental Science and Technology, Cranfield University, Bedfordshire MK43 0AL, UK.
Severn Trent Water LTD., Severn Trent Centre, PO Box 5309, Coventry CV3 9FH, West Midlands, UK.
Water Res. 2012 Nov 1;46(17):5655-5662. doi: 10.1016/j.watres.2012.07.057. Epub 2012 Aug 7.
The kinetics of photodegradation of the pesticide metaldehyde by UV/H(2)O(2) and UV/TiO(2) in laboratory grade water and a natural surface water were studied. Experiments were carried out in a bench scale collimated beam device using UVC radiation. Metaldehyde was efficiently degraded by both processes in laboratory grade water at identical rates of degradation (0.0070 and 0.0067 cm(2) mJ(-1) for UV/TiO(2) and UV/H(2)O(2) respectively) when optimised doses were used. The ratio between oxidant and metaldehyde was significantly higher for H(2)O(2) due to its low photon absorption efficiency at 254 nm. However, the presence of background organic compounds in natural water severely affected the rate of degradation, and whilst the pseudo first-order rate constant of degradation by UV/H(2)O(2) was slowed down (0.0020 cm(2) mJ(-1)), the degradation was completely inhibited for the UV/TiO(2) process (k' = 0.00007 cm(2) mJ(-1)) due to the blockage of active sites on TiO(2) surface by the background organic material.
研究了农药乌洛托品在实验室级水和天然地表水中的 UV/H2O2和 UV/TiO2光降解动力学。实验在使用 UVC 辐射的台式平行光束装置中进行。在优化剂量下,两种工艺在实验室级水中均能有效降解乌洛托品,降解速率相同(UV/TiO2和 UV/H2O2分别为 0.0070 和 0.0067 cm2 mJ-1)。由于 254nm 处 H2O2的光子吸收效率较低,氧化剂与乌洛托品的比例显著高于 H2O2。然而,天然水中背景有机化合物的存在严重影响了降解速率,尽管 UV/H2O2的降解伪一级速率常数降低(0.0020 cm2 mJ-1),但由于 TiO2表面的活性位点被背景有机物质阻塞,UV/TiO2过程完全被抑制(k' = 0.00007 cm2 mJ-1)。