高等学校化学学报 ›› 2005, Vol. 26 ›› Issue (3): 430.

• 研究论文 • 上一篇    下一篇

Co/Bi催化剂催化湿法氧化降解垃圾渗滤液中的氨氮

李鱼1, 张荣1, 李海生2, 董德明1, 刘亮1, 刘光辉1, 刘鸿亮2   

  1. 1. 吉林大学环境与资源学院,长春 130023;
    2. 北京化工大学化学化工学院,北京 100029
  • 收稿日期:2004-03-29 出版日期:2005-03-10 发布日期:2005-03-10
  • 通讯作者: 李 鱼(1965年出生),男,博士,副教授.主要从事环境污染与控制化学、环境规划与评价、环境污染物形态研究.E-mail:liyuxx@mai.ljlu.edu.cn E-mail:liyuxx@mai.ljlu.edu.cn
  • 基金资助:

    国家环保总局环境工程评估中心基金(批准号:02220100000549);吉林省环境保护补助资金(批准号:20022025)资助.

Catalytic Wet Air Oxidation of Ammonia in Landfill Leachates in the Presence of Co/Bi Catalyst

LI Yu1, ZHANG Rong1, LI Hai-Sheng2, DONG De-Ming1, LIU Liang1, LIU Guang-Hui1, LIU Hong-Liang2   

  1. 1. College of Environment and Resources, Jilin University, Changchun 130023, China;
    2. College of Chemical Engineering, Beijing University of Chemical Technology, Beijing 100029, China
  • Received:2004-03-29 Online:2005-03-10 Published:2005-03-10

摘要: 采用催化湿法氧化(CWAO)技术,以Co/Bi为催化剂,对垃圾渗滤液中氨氮(NH3-N)进行降解处理,并利用GC-MS检测了垃圾渗滤液中含氮有机物的相对含量.结果表明,随着反应温度的升高,CWAO对NH3-N的降解能力逐渐增强,在220,240,260和280℃条件下,NH3-N降解规律符合一级动力学反应(r>0.93,n=6).在升温过程(20~300℃)中,NH3-N浓度变化经历了先升后降两个阶段,并在220℃时达到最大值.GC-MS检测结果表明,在第一阶段,垃圾渗滤液中几种含氮有机物因催化氧化而生成NH3-N;第二阶段,NH3-N逐渐被氧化降解,达到了CWAO技术同时降解有机物和NH3-N的目的.同时,选取垃圾渗滤液中一种含氮有机物2-巯基苯并噻唑进行含氮有机物氮降解机理的验证实验.

关键词: 催化湿法氧化, 垃圾渗滤液, 氨氮, Co/Bi

Abstract: Catalytic Wet Air Oxidation(CWAO) was used for the decomposition of ammonia(NH3-N) from the landfill leachates in the presence of Co/Bi catalyst and the relative content of nitrogenous organic compounds in the landfill leachates was also measured by GC-MS. The results show that the decomposition ability of NH3-N by CWAO gradually increased with increasing reaction temperature. The kinetic decomposition of NH3-N at temperatures 220, 240, 260 and 280 ℃ was well described with the first-order kinetics model(r>0.93, n=6). During the overall process of temperature rising(20—300 ℃), the concentration of NH3-N increased in the first stage and then decreased in the second stage, which culminated at 220 ℃. Further investigations by GC-MS indicated that during the first stage, some nitrogenous organic compounds in the landfill leachates were degraded into NH3-N by CWAO, and then NH3-N was degraded by CWAO during the second stage, which presented the advantage of simultaneous removal of both NH3-N and organic compounds by CWAO. One of the nitrogen-organic compounds, 2-mercaptobenzothiazole, in the landfill leachates was selected to verify the degradation of the nitrogen-organic compounds.

Key words: Catalytic wet air oxidation, Landfill leachates, Ammonia-nitrogen, Co/Bi

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