Catalytic wet air oxidation of substituted phenols using activated carbon as catalyst

被引:103
作者
Suarez-Ojeda, ME
Stüber, F
Fortuny, A
Fabregat, A
Carrera, J
Font, J
机构
[1] Univ Rovira & Virgili, Dept Engn Quim, Escola Tecn Super Engn Quim, Tarragona 43007, Catalonia, Spain
[2] Univ Politecn Cataluna, Dept Engn Quim, EPSEVG, Barcelona 08800, Catalonia, Spain
[3] Univ Autonoma Barcelona, Dept Engn Quim, E-08193 Barcelona, Catalonia, Spain
关键词
activated carbon; substituted phenols; dodecylbenzene sulfonate; oxidation; trickle bed;
D O I
10.1016/j.apcatb.2004.11.017
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
Continuous catalytic wet air oxidation (CWAO) was investigated as a suitable precursor for the biological treatment of industrial wastewater that contained phenols (phenol, o-cresol, 2-chlorophenol and p-nitrophenol), aniline, sulfolane, nitrobenzene or sodium dodecylbenzene sulfonate (DBS). Seventy-two-hour tests were carried out in a fixed bed reactor in trickle flow regime, using a commercial activated carbon (AC) as catalyst. The temperature and total pressure were 140 degrees C and 13.1 bar, respectively. The influence of hydroxyl-, methyl-, chloride-, nitro-, sulfo- and sulfonic-substituents on the oxidation mechanism of aromatic compounds, the occurrence of oxidative coupling reactions over the AC, and the catalytic activity (in terms of substrate elimination) were established. The results show that the AC without any supported active metal behaves bifunctionally as adsorbent and catalyst, and is active enough to oxidate phenol, o-cresol, 2-chlorophenol and DBS, giving conversions between 30 and 55% at the conditions tested. The selectivity to the production of carbon dioxide was considerable with total organic carbon (TOC) abatement between 15 and 50%. The chemical oxygen demand (COD) reduction was between 12 and 45%. In turn, aniline, sulfolane, p-nitrophenol and nitrobenzene conversions were below 5% and there was almost no TOC abatement or COD reduction, which shows the refractory nature of these compounds. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:105 / 114
页数:10
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