期刊文献+

活性炭复合材料负载催化剂催化臭氧氧化处理石化废水 被引量:3

Treatment of petrochemical wastewater by catalytic ozone oxidation with activated carbon composite supported catalysts
在线阅读 下载PDF
导出
摘要 采用催化臭氧氧化深度处理某石化厂炼油废水,制备了活性炭复合材料负载催化剂(Fe_2O_3/ACNT),与几种常见负载催化剂进行了物性和COD去除效果的对比,并对Fe_2O_3/ACNT的催化效果和稳定性进行了详细分析。结果表明:催化剂的催化臭氧氧化活性由高到低的顺序为Fe_2O_3/ACNT>Fe_2O_3/活性炭>Fe_2O_3/Al2O3>Fe_2O_3/陶粒;Fe_2O_3/ACNT催化剂具有较高的比表面积、孔体积、强度和吸水率,使COD去除率由单独臭氧氧化时的约20%提高到66.8%。在催化剂填充量200 m L、废水pH 7.6、臭氧投加量200 mg/L、体积空速1 h^(-1)的条件下运行30d,COD去除率平均达65.1%,出水COD均值为40.8 mg/L,最高值为44.3 mg/L,满足外排水COD小于50 mg/L的指标。催化剂稳定性良好,运行30 d活性未见明显降低,具有在环保领域应用的前景。 The petrochemical wastewater was treated by catalytic ozone oxidation.The activated carbon(AC)composite supported catalyst(Fe2O3/ACNT)was prepared and compared with several common supported catalysts on physical properties and COD removal effect.The catalytic effects and stability of Fe2O3/ACNT were analyzed.The results showed that:The order of catalytic ozone oxidation activity of the catalysts was Fe2O3/ACNT>Fe2O3/AC>Fe2O3/Al2O3>Fe2O3/ceramic;Because of the higher specific area,pore volume,strength and water absorption,Fe2O3/ACNT could increase the COD removal rate from about 20%of ozone oxidation alone to 66.8%;Under the conditions of catalyst loading 200 mL,wastewater pH 7.6,ozone amount 200 mg/L,space velocity 1 h-1 and running time 30 d,the average COD removal rate was 65.1%,the average effluent COD was 40.8 mg/L and the highest value was 44.3 mg/L,which met the drainage standard(COD≤50 mg/L).The catalyst had good stability without significant activity reduction in 30 d of operation,which showed a favorable application prospect in environmental protection.
作者 赵越 蒋广安 李宝忠 马传军 王雪清 Zhao Yue;Jiang Guangan;Li Baozhong;Ma Chuanjun;Wang Xueqing(Sinopec Fushun Research Institute of Petroleum and Petrochemicals,Fushun Liaoning 113001,China)
出处 《化工环保》 CAS CSCD 北大核心 2018年第2期152-156,共5页 Environmental Protection of Chemical Industry
基金 中石化"十条龙"科技攻关项目(HB1509)
关键词 催化臭氧氧化 石化废水 活性炭 复合催化剂 catalytic ozone oxidation petrochemical wastewater activated carbon composite catalyst
  • 相关文献

参考文献5

二级参考文献96

  • 1Rivera-Utrilla J, Prados-Joya G, Sanchez-Polo M, et al. Removal of nitroimidazole antibiotics from aqueous solution by activated carbon[J]. J Jourflal of Hazardous Materials, 2009, 170: 298-305.
  • 2Kasprzyk-Hordem B, Ziblek M, Nawrocki J. Catalytic ozonation and methods of enhancing molecular ozone reactions in water treatment[J]. Applied Catalysis B: Environmental, 2003, 46(4): 639-669.
  • 3Faria P C C, Orfao J J M, Pereira M F R. A novel ceria-aetivated carbon composite for the catalytic ozonation of carboxylic acids[J]. CatalysisCommunications, 2008, 9:2121-2126.
  • 4Faria P C C, Orfao J J M, Pereira M F R. Catalytic ozonation ofsulfonated aromatic compounds in the presence of activated carbon[J]. Applied Catalysis B: Environmental, 2008, 83: 150-159.
  • 5Xukai Li, Qiuyun Zhang, Lili Tang, et al. Catalytic ozonation of p-chlorobenzoic acid by activated carbon and nickel supported activated carbon prepared from petroleum coke[J]. Journal of Hazardous Materials, 2009, 163: 115-120.
  • 6Laisheng Li, Weiying Ye, Qiuyun Zhang, et al. Catalytic ozunation of dimethyl phthalate over cerium supported on activated carbon[J]. Journal of Hazardous Materials, 2009, 170: 411-416.
  • 7Sanchez-Polo M, von Gunten U, Rivera-Utrilla J. Efficiency of activated carbon to transform ozone into -OH radicals: Influence of operational parameters[J]. Water Research, 2005, 39(14): 3189-3198.
  • 8Hoigne J, Bader H. Rate constants of reaction of ozone with organic and inorganic compounds in water I : Dissociating organic compounds[J]. Water Research, 1983, 17: 173-183.
  • 9Hoigne J, Bader H. Rate constants of reaction of ozone with organic and inorganic compounds in waterll: Dissociating organic compounds[J]. Water Research, 1983, 17: 185-194.
  • 10G V Buxton. Critical review of rate constants for reactions of hydrated electrons, hydrogen atoms and hydroxyl radicals in aqueous solution[J]. Journal of Physical and Chemical Reference Data, 1988, 17: 513-594.

共引文献35

同被引文献49

引证文献3

二级引证文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部