Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
580034 | Journal of Hazardous Materials | 2010 | 5 Pages |
Abstract
The degradation mechanism of p-nitrophenol (p-NP) exposed to 254Â nm UV light was studied in the presence and the absence of oxygen respectively via both steady-state photolysis and time-resolved laser flash photolysis (LFP) experiments. It has been confirmed that p-NP can be photo-ionized to produce its radical cation (p-NP+) and hydrated electron (eaqâ) with a quantum yield of 0.52. In neutral solution p-NP+ will be quickly deprotonated to form its phenoxyl radical (p-NP) which will react with oxygen to promote the breakage of benzene ring of p-NP. The degradation efficiency of p-NP exposed to 254Â nm UV is as low as commonly reported. However, oxygen could improve the photo-degradation efficiency, which is due to the reaction of oxygen with p-NP. The reaction between oxygen and p-NP has been experimentally confirmed both in LFP and in pulse radiolysis.
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Authors
Sufang Zhao, Hongjuan Ma, Min Wang, Changqing Cao, Jie Xiong, Yunshu Xu, Side Yao,