Aqueous-phase nitration of phenol by N2O5 and ClNO2

被引:53
作者
Heal, Mathew R.
Harrison, Mark A. J.
Cape, J. Neil
机构
[1] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
[2] Edinburgh Res Stn, Ctr Ecol & Hydrol, Penicuik EH26 0QB, Midlothian, Scotland
基金
英国自然环境研究理事会;
关键词
tropospheric chemistry; heterogeneous chemistry; nitrosation; nitronium ion;
D O I
10.1016/j.atmosenv.2007.02.003
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nitrophenols are present in the atmospheric gas phase and in cloud and rainwater. Their formation via aqueous-phase reactions of phenol with the nitronium ion, NO2+, arising from N2O5 and ClNO2 partitioning into the aqueous phase, has been proposed but not verified experimentally. Here, we demonstrate for the first time that gaseous N2O5 and ClNO2 partitioning into dilute aqueous solutions of phenol yields 2- and 4-nitrophenol (and 4-nitrosophenol), but no dinitrophenol isomers. The rate of nitration does not vary significantly between 5 and 20 degrees C, presumably because of opposing temperature dependences in Henry's law partitioning and reaction rate coefficients. The rate coefficient for reaction of NO2+ with phenol Could not be directly quantified but is evidently large enough for this reaction to compete effectively with the reaction between NO2+ and water and to provide a feasible route to nitrophenol production in the atmosphere. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3515 / 3520
页数:6
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