The role of nitrite and nitrate ions as photosensitizers in the phototransformation of phenolic compounds in seawater

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• 作者：P. Calza^a ; ^{paola.calza@unito.it} ; ; D. Vione^a ; ^b ; ; A. Novelli^c ; E. Pelizzetti^a ; ; C. Minero^a ;
• 关键词：Nitrite ; Phenol ; Chlorophenols ; Nitrophenol ; Photodegradation ; Seawater
• 刊名：Science of the Total Environment
• 出版年：2012
• 出版时间：15 November, 2012
• 年：2012
• 卷：439
• 期：Complete
• 页码：67-75
• 全文大小：1036 K

文摘

Nitrite and nitrate are known to be involved in photochemical processes occurring in natural waters. In this study we have investigated the role played by these photosensitizers towards the transformation of xenobiotic organic matter in marine water, with the goal of assessing the typical transformation routes induced in seawater by irradiated nitrite/nitrate. For this purpose, phenol was chosen as model molecule. Phenol transformation was investigated under simulated solar radiation in the presence of nitrite (in the range of 1 ¡Á 10^? 5-1 ¡Á 10^? 2 M) or nitrate ions, in pure water at pH 8, in artificial seawater (containing same dissolved salts as seawater but no organic matter), and in natural seawater. In all experiments, phenol degradation rate and formation of intermediates were assessed. As expected, phenol disappearance rate decreased with decreasing nitrite concentration and was slightly reduced by the presence of chloride. Other salts present in artificial seawater (e.g. HCO₃^?, CO₃^2 ? and Br^?) had a more marked effect on phenol transformation. Analysis of intermediates formed in the different matrices under study showed generation of hydroxyl-, nitro- and chloroderivatives of phenol, to a different extent depending on experimental conditions. 1,4-Benzoquinone prevailed in all cases, nitroderivatives were only formed with nitrite but were not detected in nitrate-spiked solutions. Competition was observed between halogenation and nitration of phenol, with variable outcome depending on nitrite concentration. The most likely reason is competition between nitrating and halogenating species for reaction with the phenoxyl radical. A kinetic model able to justify the occurrence of different intermediates under the adopted conditions is presented and discussed.