期刊文献+

β-FeOOH/蜂窝陶瓷催化臭氧化高效去除饮用水中有机污染物 被引量:2

Efficient removal of organic pollutants in drinkingwater by catalytic ozonation catalyst β-FeOOH/ceramic honeycomb
原文传递
导出
摘要 市售蜂窝陶瓷经过氧化铝涂层后,进一步负载β-FeOOH活性组分,制得改性蜂窝陶瓷催化剂(β-FeOOH/Ce-ramic honeycomb,β-FeOOH/CH)。与单独臭氧氧化相比,基于该催化剂的固定床反应装置体现出更好的臭氧化活性,反应20 min后,水中的2,4-二氯苯氧乙酸(2,4-D)就可以完全去除,其矿化效率也可以达到80%以上。进一步考察了进水流速、有机物浓度等因素对多相催化臭氧化效率的影响,结果表明:β-FeOOH/CH可以显著提高臭氧的利用效率,能够有效去除水中包括2,4-D在内的多种有机污染物,而且催化剂可以重复使用,在长期的运行实验中其催化性能没有明显下降,该反应装置在饮用水深度处理领域具有很好的应用潜力。 β-FeOOH/ceramic honeycomb(β-FeOOH/CH) was prepared by the following procedure: ceramic honeycomb was washcoated by Al2O3 via sol-gel method with boehmite as precursor,which was further modified by loading β-FeOOH(as active species).In comparison with ozonation process,the catalyst exhibited a higher catalytic activity for the degradation of 2,4-dichlorophenoxyacetic acid(2,4-D) in a semi-continuous laboratory reactor.At a reaction time of 20 min,2,4-D was completely destroyed and about 80% of the TOC was removed under the optimum conditions.Moreover,the effects of water flow speed and the initial concentration of organic pollutants et al.on the catalytic ozonation efficiency were also studied in detail.The results indicated that ozone could be efficiently decomposed over β-FeOOH/CH,leading to the highly efficient removal of organic pollutants such as atrazine and epichlorohydrin.Furthermore,β-FeOOH/CH had an excellent long-term stability and no obviously deactivation in 30 successive cycles.Therefore,β-FeOOH/CH has a promising application in drinking water treatment.
出处 《环境工程学报》 CAS CSCD 北大核心 2012年第10期3378-3382,共5页 Chinese Journal of Environmental Engineering
基金 国家高技术研究发展计划(863)项目(2008AA06A414) 国家自然科学基金资助项目(50908223)
关键词 蜂窝陶瓷(CH) 催化臭氧化 有机污染物 去除 ceramic honeycomb(CH) catalytic ozonation organic pollutant removal
  • 相关文献

参考文献13

  • 1Piera E.,Calpe J. C.,Brillas E. , et al. 2,4-dichloro-phenoxyacetic acid degradation by catalyzed ozonation :TiO2/UV/03and Fe (11)/UV/03 systems. Appl. Catal.B: Environ. , 2000,27(3) : 169-177.
  • 2Zona R.,Solar S.,Gehringer P. Degradation of 2,4-di-chlorophenoxyacetic acid by ionizing radiation : Influence ofoxygen concentration. Wat. Res.,2002, 36(5):1369-1374.
  • 3Chu W.,Chan K. H.,Kwan C. Y. Modeling the ozona-tion of herbicide 2,4-D through a kinetic approach. Chem-osphere, 2004,55(5) :647-652.
  • 4Beltran F. J.,Rivas F. J.,Montero-D-Espinosa R. Cata-lytic ozonation of oxalic acid in an aqueous TiO2 slurry re-actor. Appl. Catal. B:Eviron.,2002,39 (3) :221 -232.
  • 5Ma J.,Graham N. J. D. Degradation of atrazine by man-ganese-catalyzed ozonation : Influence of humic substances.Wat. Res.,1999,33(3):785-793.
  • 6Ma J.,Graham N. J. D. Preliminary investigation of man-ganese-catalyzed ozonation for the destruction of atrazine.Ozone: Sci. Eng. , 1997,19(3) ;227-240.
  • 7Ma J.,Graham N. J. D. Degradation of atrazine by man-ganese-catalyzed ozonation: Influence of radical scaven-gers. Wat. Res.,2000,34(15):3822-3828.
  • 8Ernst M.,Lurot F.,Schrotter J. C. Catalytic ozonation ofrefractory organic model compounds in aqueous solution byaluminum oxide. Appl. Catal.,2004,47( 1) : 15-25.
  • 9Karpel Vel Leitner N.,Delouane B.,Legube B.,et al.Effect of catalysts during ozonation of salicylic acid, pep-tides and humic substances in aqueous solution. Ozone :Sci. Eng.,1999,21(3) : 261-276.
  • 10Gracia R.,Cortes S.,Sarasa J.,et al. Catalytic ozona-tion with supported titanium dioxide. The stability of cata-lyst in water. Ozone: Sci. Eng.,2000,22(2) : 185-193.

二级参考文献17

共引文献21

同被引文献19

引证文献2

二级引证文献12

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