Catalytic wet air oxidation of wastewater containing ammonia and phenol over activated carbon supported Pt catalysts

被引:82
作者
Cao, SL [1 ]
Chen, GH [1 ]
Hu, XJ [1 ]
Yue, PL [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Chem Engn, Hong Kong, Hong Kong, Peoples R China
关键词
catalysts; base metals; noble metals; wastewater; landfill leachate;
D O I
10.1016/j.cattod.2003.08.005
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Noble metal catalysts on activated carbon (AC) (Pt/AC and Ru/AC) and base metal catalysts (Cu/AC, CoMo/AC, Mo/AC, Mn/AC, Ru/Al2O3) were developed and examined for the simultaneous removal of organic pollutants and ammonia from wastewater using the wet air oxidation (WAO) process in the liquid phase. The noble metal catalysts were much more active than were the base metal catalysts. Ammonia removal was the rate-controlling step. Nitrate and nitrite accounted for a minor portion of the decomposed ammonia (<5% for Ru/AC and <3% for Pt/AC). Pt/AC was superior to Ru/AC in terms of ammonia removal, pH sensitivity and stability. Activated carbon was a better support for Pt than was TiO2, Al2O3 or MCM-41. The optimal preparation conditions of Pt/AC were: calcination at 300 degreesC for 6 h followed by H-2 reduction at 600 degreesC without pretreatment of AC. The catalyst so prepared, Pt(opt)/AC, produced ammonia removals of 52 and 88% at 200 degreesC, initial pH of 5.6 and 12, respectively. The experimental results based on the Pt(opt)/AC showed that the Pt/AC catalyst was able to remove ammonia (>50%) and phenol (approximate to100%) simultaneously from highly polluted wastewater containing up to 1500 mg/l N ammonia and up to 8000 mg/l COD. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 47
页数:11
相关论文
共 30 条
[11]   WET OXIDATION OF OXYGEN-CONTAINING AND NITROGEN-CONTAINING ORGANIC-COMPOUNDS CATALYZED BY COBALT(III) OXIDE [J].
ITO, MM ;
AKITA, K ;
INOUE, H .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1989, 28 (07) :894-899
[12]   Kinetics of oxidation of ammonia in solutions containing ozone with or without hydrogen peroxide [J].
Kuo, CH ;
Yuan, F ;
Hill, DO .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1997, 36 (10) :4108-4113
[13]   Catalytic wet air oxidation of dyeing and printing wastewater [J].
Lei, L ;
Hu, X ;
Chu, HP ;
Chen, G ;
Yue, PL .
WATER SCIENCE AND TECHNOLOGY, 1997, 35 (04) :311-319
[14]   GENERALIZED KINETIC-MODEL FOR WET OXIDATION OF ORGANIC-COMPOUNDS [J].
LI, LX ;
CHEN, PS ;
GLOYNA, EF .
AICHE JOURNAL, 1991, 37 (11) :1687-1697
[15]   Selective NH3 oxidation to N-2 in a wet stream [J].
Li, YJ ;
Armor, JN .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1997, 13 (02) :131-139
[16]   Characterization and reactivity of MoO3/SiO2 catalysts in the selective catalytic oxidation of ammonia to N2 [J].
Lietti, L ;
Ramis, G ;
Busca, G ;
Bregani, F ;
Forzatti, P .
CATALYSIS TODAY, 2000, 61 (1-4) :187-195
[17]   Oxime inhibition of nitrification during treatment of an ammonia-containing industrial wastewater [J].
Love, NG ;
Smith, RJ ;
Gilmore, KR ;
Randall, CW .
WATER ENVIRONMENT RESEARCH, 1999, 71 (04) :418-426
[18]  
Okada N., 1977, U.S. Patent, Patent No. 4141828
[19]   Catalytic wet air oxidation of ammonia over alumina supported metals [J].
Qin, JY ;
Aika, K .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 16 (03) :261-268
[20]   VAPOR-LIQUID-EQUILIBRIUM DATA FOR THE NH3-H2O SYSTEM AND ITS DESCRIPTION WITH A MODIFIED CUBIC EQUATION OF STATE [J].
SMOLEN, TM ;
MANLEY, DB ;
POLING, BE .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1991, 36 (02) :202-208