Shanghai Institute of Applied Physics, Chinese Academy of Sciences, P. O. Box 800-204, Shanghai, 201800, PR China.
Photochem Photobiol Sci. 2010 May;9(5):710-5. doi: 10.1039/b9pp00187e. Epub 2010 Mar 22.
The degradation kinetics of p-nitrophenol (p-NP) exposed to 254/185 nm UV light were studied in two modes, i.e., 254 nm UV light intensity enhanced mode and normal mode. It was observed that the extra 254 nm UV light source accelerated the degradation process both in the presence and the absence of oxygen. Considering that hydroxyl radical (*OH) is the dominant factor that causes the degradation of p-NP, the enhanced degradation that occurred in the presence of the extra light source was attributed to the synergistic effect between *OH attack and the primary reactions initiated by 254 nm UV light. The synergistic effect has been confirmed by 266 nm laser flash photolysis (LFP) experiments. It is demonstrated that the phenoxy radical generated from the photoionization of p-NP is capable of reacting with *OH. On the basis of these results, it should be noted that UV light could cause more severe damage to p-NP attacked by *OH in aqueous solution.
研究了 254/185nmUV 光照射下 p-硝基苯酚(p-NP)的降解动力学,分别在增强 254nmUV 光强度模式和正常模式下进行。结果表明,额外的 254nmUV 光源在有氧和无氧条件下均加速了降解过程。考虑到羟基自由基(OH)是导致 p-NP 降解的主要因素,额外光源存在时增强的降解归因于OH 攻击和 254nmUV 光引发的初级反应之间的协同效应。协同效应已通过 266nm 激光闪光光解(LFP)实验得到证实。实验表明,p-NP 光离子化产生的苯氧基自由基能够与OH 反应。基于这些结果,应该注意到,在水溶液中,UV 光可能会对OH 攻击的 p-NP 造成更严重的破坏。