Highly efficient application of activated carbon as catalyst for wet peroxide oxidation

被引:91
作者
Dominguez, C. M. [1 ]
Ocon, P. [2 ]
Quintanilla, A. [1 ]
Casas, J. A. [1 ]
Rodriguez, J. J. [1 ]
机构
[1] Univ Autonoma Madrid, Area Ingn Quim, E-28049 Madrid, Spain
[2] Univ Autonoma Madrid, Fac Ciencias Quim, Dept Quim Fis Aplicada, E-28049 Madrid, Spain
关键词
Activated carbon; Hydrogen peroxide; Cyclic voltammetry; Catalytic wet peroxide oxidation; Regeneration; HYDROGEN-PEROXIDE; ORGANIC CONTAMINANTS; AQUEOUS-SOLUTION; PHENOLIC-COMPOUNDS; AIR OXIDATION; DECOMPOSITION; SURFACE; H2O2; 4-CHLOROPHENOL; REGENERATION;
D O I
10.1016/j.apcatb.2013.04.068
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This paper addresses the improved performance of activated carbons in catalytic wet peroxide oxidation (CWPO) of phenol as target compound. Initial cyclic voltammetry experiments show that hydrogen peroxide and phenol compete for the same active sites on the carbon surface. Then, a significant coverage of the carbon surface by phenol molecules is the approach attempted to increase the efficiency of hydrogen peroxide and the performance of the oxidation process. In this work, two commercial activated carbons, with different physical and electrochemical properties have been tested. The results demonstrate that working at high phenol concentration (5 g/L) and phenol/carbon mass ratio (2), unprecedented hydrogen peroxide efficiencies of around 100% are achieved, allowing high oxidation and mineralization degrees, i.e. 97% phenol and 70% TOC conversions at 80 degrees C with the stoichiometric dose of hydrogen peroxide required for complete mineralization of phenol. The oxidation route of phenol in the presence of activated carbon is also studied and a reaction pathway proposed. Resorcinol was a new by-product detected whose formation occurs upon reaction on the carbon surface. Condensation by-products, typically formed in Fenton oxidation of phenol, were not found in the effluents but adsorbed on the carbon surface causing a progressive deactivation upon use. The activity can be easily recovered by oxidative thermal regeneration (350 degrees C, 24 h). (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:663 / 670
页数:8
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