Evolution of toxicity upon wet catalytic oxidation of phenol

被引:152
|
作者
Santos, A
Yustos, P
Quintanilla, A
García-Ochoa, F
Casas, JA
Rodríguez, JJ
机构
[1] Univ Complutense Madrid, Fac Ciencias Quim, Dept Ingn Quim, Madrid 28040, Spain
[2] Univ Autonoma Madrid, Madrid 28049, Spain
关键词
D O I
10.1021/es030476t
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This work reports on the evolution of the toxicity of phenol-containing simulated wastewater upon catalytic wet oxidation with a commercial copper-based catalyst (Engelhard Cu-0203T). The results of the study show that this catalyst enhances detoxification, in addition to its effect on the oxidation rate. The EC50 values of the intermediates identified throughout the oxidation route of phenol have been determined and used to predict the evolution of toxicity upon oxidation. The predicted values have been compared with the ones measured directly from the aqueous solution during the oxidation process. To learn about the evolution of toxicity throughout the routes of phenol oxidation, experiments have been performed with simulated wastewaters containing separately phenol, catechol, and hydroquinone as original pollutants, The significant increase of toxicity observed during the early stages of phenol oxidation is not directly related to the development of the brown color that derives mainly from catechol oxidation. This increase of toxicity is caused by the formation of hydroquinone and p-benzoquinone as intermediates, the former showing the highest toxicity. Furthermore, synergistic effects, giving rise to a significant increase of toxicity, have been observed. These effects derive from the interactions among copper leached from the catalyst and catechol, hydroquinone, and p-benzoquinone and demand that close attention be paid to this potential problem in catalytic wet oxidation.
引用
收藏
页码:133 / 138
页数:6
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