Catalytic liquid phase oxidation of aqueous phenol solutions in a trickle-bed reactor

被引:61
作者
Pintar, A [1 ]
Bercic, G [1 ]
Levec, J [1 ]
机构
[1] UNIV LJUBLJANA, DEPT CHEM ENGN, SI-1001 LJUBLJANA, SLOVENIA
关键词
heterogeneous catalysis; liquid-phase oxidation; aqueous phenol solution; metal oxide catalysts; trickle-bed reactor modelling; waste water treatment;
D O I
10.1016/S0009-2509(97)00257-1
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Aqueous-phase deep oxidation at comparatively low temperatures and pressures made possible by the use of heterogeneous catalysts is a promising technique for the destruction of organic water pollutants. Catalytic liquid-phase oxidation of aqueous phenol solutions was investigated in an isothermal trickle-bed reactor at T = 403-423 K and oxygen partial pressure of 7 bar. The results obtained in the presence of a catalyst composed of supported copper, zinc, and cobalt oxides show that during the reaction course only small amounts of aromatic and aliphatic hydrocarbons are accumulated in the liquid phase, thus resulting to a constant pH value of the aqueous solution along the axial reactor coordinate. In the off-gas, no carbon monoxide was detected at any operating conditions. Process simulating using one-dimensional axial dispersion and plug-flow models demonstrates that efficiency of the catalyst bed for phenol removal is influenced by the mass-transfer rate of oxygen from the gas phase to the bulk liquid phase, and by resistance due to a surface reaction step. It is believed that partial wetting of catalyst particles in a trickle-bed reactor increases phenol conversion to intermediates and CO2 as the main reaction product, through the formation of a larger number of active sites on the catalyst surface. Finally, it has been observed that at the given operating conditions metal oxide phases are leached into the aqueous solution. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:4143 / 4153
页数:11
相关论文
共 29 条
[1]  
BAILLOD CR, 1982, ENVIRON PROG, V1, P217
[2]  
Chowdhury AK, 1975, AICHE S SER, V71, P46
[3]   MECHANISM OF THE OXIDATION OF AQUEOUS PHENOL WITH DISSOLVED-OXYGEN [J].
DEVLIN, HR ;
HARRIS, IJ .
INDUSTRIAL & ENGINEERING CHEMISTRY FUNDAMENTALS, 1984, 23 (04) :387-392
[4]   Catalytic oxidation in supercritical water [J].
Ding, ZY ;
Frisch, MA ;
Li, LX ;
Gloyna, EF .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1996, 35 (10) :3257-3279
[5]   Catalytic oxidation of organic compounds in aqueous media [J].
Duprez, D ;
Delanoe, F ;
Barbier-Jr, J ;
Isnard, P ;
Blanchard, G .
CATALYSIS TODAY, 1996, 29 (1-4) :317-322
[6]   CATALYTIC REMOVAL OF PHENOL FROM AQUEOUS-PHASE USING OXYGEN OR AIR AS OXIDANT [J].
FORTUNY, A ;
FERRER, C ;
BENGOA, C ;
FONT, J ;
FABREGAT, A .
CATALYSIS TODAY, 1995, 24 (1-2) :79-83
[7]  
Gallezot P, 1996, APPL CATAL B-ENVIRON, V9, pL11
[8]   ELECTROLYTIC DECOMPOSITION AND PHOTO-DECOMPOSITION OF COMPOUND SEMICONDUCTORS IN CONTACT WITH ELECTROLYTES [J].
GERISCHER, H .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY, 1978, 15 (04) :1422-1428
[9]   TRICKLE-BED REACTOR PERFORMANCE .1. HOLDUP AND MASS-TRANSFER EFFECTS [J].
GOTO, S ;
SMITH, JM .
AICHE JOURNAL, 1975, 21 (04) :706-713
[10]   TRICKLE-BED REACTOR PERFORMANCE .2. REACTION STUDIES [J].
GOTO, S ;
SMITH, JM .
AICHE JOURNAL, 1975, 21 (04) :714-720