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微波诱导Fe_2O_3/Al_2O_3催化剂催化氧化处理水中苯酚 被引量:40

Microwave-Induced Catalytic Oxidation Process for Treatment of Phenol in Water with Fe_2O_3/Al_2O_3 Catalyst
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摘要 以γ-Al_2O_3为载体,采用浸渍焙烧法制备了Fe_2O_3/Al_2O_3催化剂,并将其应用于微波诱导催化氧化处理模拟含酚废水.X射线衍射和X射线荧光光谱测试结果表明,活性组分氧化铁在催化剂中以α-Fe_2O_3的形式存在,其含量为3.71%.与载体氧化铝相比,Fe_2O_3/Al_2O_3催化剂的比表面积和平均孔径及平均孔容略有降低.对于100mg/L的模拟含酚废水,最佳的处理工艺条件为微波辐照功率400W,辐照时间5min,催化剂加入量60g/L,H_2O_2浓度600mg/L,体系pH>4.在此工艺条件下,水中苯酚的去除率达97.98%.催化剂连续使用20次后苯酚去除率仍达96.34%.表观反应动力学研究表明,在氧化铁催化剂存在的条件下,微波诱导H2O2产生氧化性极强的羟基自由基,整个反应过程可分为微波诱导阶段和催化氧化阶段,两个阶段的氧化过程均符合一级反应动力学规律. The ferric oxide catalyst was prepared by the dipping- calcination method using gamma-Al2O3 as a carrier and the microwave- induced oxidation process was developed to treat phenol in water. The catalyst structure was determined by XRD, XRF and N-2 adsorption. The effects of operating conditions on the catalyst activity, the using life of the catalyst and the reaction kinetics were studied. The results show that alpha-Fe2O3 is loaded on the surface of gamma-Al2O3 and the content of alpha-Fe2O3 in the catalyst is 3.71 %. Under the optimal treatment conditions of phenol concentration of 100 mg/L, microwave power of 400 W, irradiation time of 5 min, catalyst amount of 60 g/L, H2O2 concentration of 600 mg/L and pH > 4, a phenol removal rate of 97.98% is obtained. The catalyst can be reused more than 20 times remaining a phenol removal rate of 96. 34 %. The oxidation process can be divided into two stages, both of them are in accord with the first-order reaction kinetics.
出处 《催化学报》 SCIE CAS CSCD 北大核心 2005年第7期597-601,共5页
基金 国家自然科学基金资助项目(50278023) 高等学校博士学科点专项科研基金资助课题(20040213027) 黑龙江省自然科学基金资助项目(E0211).
关键词 微波诱导氧化工艺 过氧化氢 氧化铁 氧化铝 负载型催化剂 苯酚 废水处理 microwave-induced oxidation process hydrogen peroxide ferric oxide alumina supported catalyst phenol wastewater treatment
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  • 1孙加飞,马军,隋军.气相色谱法测定水中痕量硝基苯[J].理化检验(化学分册),1993,29(5):275-277. 被引量:7
  • 2何绪文.煤气发生站洗冷废水治理研究[J].环境污染与防治,1996,18(5):5-7. 被引量:4
  • 3[2]ZHANG Xunli, HAYWARD D O, LEE C, et al. Microwave assisted catalytic reduction of sulfur dioxide with methane over MoS2 catalysts [ J ]. Applied Catalysis B: Environmental, 2001,33:137 - 148.
  • 4[3]JONES D A, LELYVELD T P, MAVROFIDIS S D, et al. Microwave heating application in environmental engineering - a review [ J ]. Resources, conservation and recycling, 2002,34:75 - 90.
  • 5[1]Beltrán FJ, Rivas FJ, Mon tero-de-Espinosa R. Catalytic ozonation of oxalic acid in an aqueous TiO2 slurry reactor[J]. Applied Catalysis B: Environmental, 2002, 39: 221~231.
  • 6[2]Andreozi R, Insola A, Gaprio V, Marotta R, Tufano V. The use of manganese dioxide as a heterogeneous catalyst for oxalic acid ozonation in aqueous solution[J]. Applied Catalysis A: General, 1996,138:75~81.
  • 7[3]Andreozzi R, Caprio V, Insola A, Marotta R, Tufano V. The ozonation of pyruvic acid in aqueous solutions catalyzed by suspended and dissolved manganese[J]. Water Research, 1998, 32(5):1492~1496.
  • 8[4]Naydenov A, Mehandjiev D. Complete oxidation of benzene on manganese dioxide by ozone[J]. Applied Catalysis A: General, 1993, 97:17~22.
  • 9[5]Legube B, Leitner NKV. Catalytic ozonation: a promising advanced oxidation technology for water treatment[J]. Catalysis Today, 1999, 53:61~72.
  • 10[6]Delano?c F, Acedo B, Leintner KV, Legube B. Relationship between the structure of Ru/CeO2 catalysts and their activity in the catalytic ozonation of succinic acid aqueous solutions[J]. Applied Catalysis B: Environmental, 2001, 29:315~325.

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