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超声场下制备催化燃烧VOCs的CuO/γ-Al_2O_3催化剂 被引量:15

Preparation of CuO/ γ -Al_2O_3 Catalysts with Ultrasonic Treatment for Catalytic Combustion of VOCs
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摘要 对在超声场下制备得到的CuO/γ-Al2O3催化剂与常规的浸渍法制备的CuO/γ-Al2O3催化剂进行了对比研究,分别进行催化氧化(燃烧)销毁甲苯和苯的实验,并用SEM,XRD,TPR和XPS对所制备的催化剂进行表征。研究结果表明:使用超声场下制备得到的CuO/γ-Al2O3作为催化剂的活性明显高于普通浸渍法制备得到的CuO/γ-Al2O3催化剂的活性。SEM分析表明,在超声场下制备的CuO/γ-Al2O3催化剂表面上的CuO晶体颗粒较小,且分布均匀;XRD分析表明超声促进了活性组分铜在表面的分散,CuO在催化剂表面由晶体向高分散的非晶相型转变。TPR分析表明在超声场下制备的CuO/γ-Al2O3催化剂中活性组分铜还原的途径从Cu(Ⅱ)还原到Cu(Ⅰ),再从Cu(Ⅰ)还原到金属铜,这有助于增强催化剂中Cu的还原性;XPS表征分析显示,在超声场下制备的CuO/γ-Al2O3催化剂与用普通浸渍法制得的CuO/γ-Al2O3相比,Cu2p3/2的结合能由934.2eV变到933.1eV,在催化剂表面呈现出Cu2+和Cu+的混合形式。 Besides using the conventional impregnation method, the CuOγ -Al2O3 catalysts, which are used for catalytic combustion of volatile organic compounds (VOCs), were also prepared separately by the impregnation method assisted with ultrasonic treatment. Using these catalysts prepared , the catalytic combustions of two kinds of VOCs, toluene and benzene, were carried out experimentally. The surface properties of these catalysts were characterized by scanning electron micrograph (SEM), X-ray diffraction (XRD), temperature-programmed reduction with H2 (H2-TPR) and X-ray photoelectron spectroscopy (XPS). The experimental results show that during catalytic combustion of VOCs, the activity of the CuO/γ -Al2O3 catalysts prepared with using ultrasonic treatment is much higher than that of prepared by conventional impregnation method. SEM shows that the use of ultrasound makes the CuO particle size of CuO/γ -Al2O3 catalyst prepared with using ultrasound much smaller than that of prepared by conventional impregnation method. XRD results show that the use of ultrasound causes the Cu ions highly disperse on the CuO/γ -Al2O3 catalysts. TPR shows that ultrasound makes the CuO reduction occurs in two steps, that is from Cu(Ⅱ ) to Cu(Ⅰ) and then from Cu(Ⅰ) to metallic copper. XPS analysis indicates that comparing with the CuO/γ -Al2O3 catalysts prepared by conventional impregnation method, the binding energy level of the catalysts prepared with using ultrasound decrease from 934.2 eV to 933.1 eV, which indicates that the Cu existing on the catalyst surface is in the form of Cu^2+ and Cu^+.
出处 《高校化学工程学报》 EI CAS CSCD 北大核心 2006年第3期368-373,共6页 Journal of Chemical Engineering of Chinese Universities
基金 国家自然科学基金重点项目(20336020) 教育部博士点基金(20020561010)。
关键词 超声场 催化剂 催化燃烧 挥发性有机物 ultrasound catalyst catalytic combustion volatile organic compounds.
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参考文献19

  • 1吴永文,李忠,奚红霞,徐科峰,韩静磊,郭建光.VOCs污染控制技术与吸附催化材料[J].离子交换与吸附,2003,19(1):88-95. 被引量:52
  • 2牛学坤,陈标华,李成岳,周集义.流向变换催化燃烧反应器的可操作性[J].化工学报,2003,54(9):1235-1239. 被引量:12
  • 3应卫勇,廖仕杰,房鼎业,Kameyama Hideo.新型催化剂上甲苯、丙烯、一氧化碳催化燃烧反应动力学[J].化工学报,2002,53(10):1051-1055. 被引量:7
  • 4Jeffrey Chi-Sheng Wu.VOCs deep oxidation over Pt catalysts using hydrophobic supports[J].Catalysis Today,1998,44(4):111-118.
  • 5Gabriele C.Supported palladium catalysts in environmental catalytic technologies for gaseous emissions[J].Journal of Molecular Catalysis A:Chemical,2001,173(2):287-312.
  • 6Parida K M.Catalytic combustion of volatile organic compounds on Indian Ocean manganese nodules[J].Applied Catalysis A:General,1999,182(2):249-256.
  • 7Taylor S H,Heneghan C S,Hutchings G J.The activity and mechanism of uranium oxide catalysts for the oxidative destruction of volatile organic compounds[J].Catalysis Today,2000,59(3):249-259.
  • 8郭建光,李忠,奚红霞,何余生,王伯光.催化燃烧VOCs的三种过渡金属催化剂的活性比较[J].华南理工大学学报(自然科学版),2004,32(5):56-59. 被引量:36
  • 9Finocchio E,Baldi M.A study of the abatement of VOC over V2O5-WO3-TiO2 and alternative SCR catalysts[J].Catalysis Today,2000,59(4):261-268.
  • 10Róbert Auer,Mihai Alifanti.Catalytic combustion of methane in the presence of organic and inorganic compounds over La0.9Ce0.1CoO3 catalyst[J].Applied Catalysis B:Environmental,2002,39(4):311-318.

二级参考文献53

  • 1林仲茂.声化学发展概况[J].应用声学,1993,12(1):1-5. 被引量:45
  • 2单绍纯,封雷,孙鸣鸣,伏义路.甲苯完全氧化反应中含铬催化剂的TPR研究[J].Chinese Journal of Catalysis,1994,15(2):134-137. 被引量:6
  • 3徐清才,黄培泉,李忠.CR型吸附剂对蔗糖和还原糖的吸附特性[J].高校化学工程学报,1994,8(1):78-83. 被引量:2
  • 4董林,陈懿.一些离子化合物在CeO_2和γ-Al_2O_3载体上的分散嵌入模型的新证据[J].Chinese Journal of Catalysis,1995,16(2):85-86. 被引量:7
  • 5Eigenberger G, Nieken U. Catalytic Combustion With Periodic Flow Reversal. Chem Eng Sci, 1988, 43(8): 2109-2115.
  • 6Cunill E, Van de Beld L, Westerterp K R. Catalytic Combustion of Very Lean Mixtures in a Reverse Floe Reactor Using an Internal Electrical Heater. Ind Eng Chem Res, 1997, 36 (10):4198-4206.
  • 7Van de Beld L, Westerterp K R. Operation of a Catalytic Reverse Flow Reactor For the Purifieation of Air Contaminated With Volatile Orgarfic Compounds. Can J Chem Eng, 1996,74: 566-573.
  • 8Van de Beld L, Borman R A, Derkx O R, Van Woezik B A A,Westerterp K R. Removal of VOCs from Polluted Air in a Reverse Flow Reactor: an Experiment Study. Ind Eng Chem Res,1994, 33(12) : 2946-2956.
  • 9Van de Beld L, Bijl M P G, Reiders A, Van de Beld L,Westerterp K R. The Catalytic Oxidation of Organic Contaminants in a Packed Bed Reactor. Chem Eng Sci. 1994, 49 (24) :4361-4373.
  • 10Van de Beld L, Westerterp K R. Air Purification in a Reverse Flow Reactor: Model Simulations vs. Experiments. AIChE J,1996, 42(4): 1139-1148.

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