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Mechanism study on CO-SCR over Ce-Co-Ox mixed oxides catalysts |
FU Yu-xiu1, ZHONG Xue-mei1, CHANG Hua-zhen1, LI Jun-hua2 |
1. School of Environment & Natural Resource, Renmin University of China, Beijing 100872, China;
2. School of Environment, Tsinghua University, Beijing 100084, China |
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Abstract In this paper, a series of Ce-Co-Ox catalysts were prepared by co-precipitation method and the CO-SCR performance was studied. The influence of Co and Ce ratio on the activity of CO-SCR was investigated and the Ce(0.3)-Co(0.7)-Ox sample showed the highest NO conversion efficiency of 84% at 250℃. According to characterization results, it was proposed that the active sites for CO-SCR is Co in Ce(0.3)-Co(0.7)-Ox. There were two reasons responsible for the enhanced catalytic performance by Ce doping into the Ce-Co-Ox catalyst. Firstly, the specific surface area and adsorption capacity were increased with Ce doping. Secondly, a solid solution was formed in Ce-Co-Ox catalyst, resulting in the enhanced oxygen migration rate. In situ DRIFTs results suggested that the CO-SCR is likely to follow a mechanism that gaseous or weakly-adsorbed CO reacts with adsorbed NO species in the forms of bridging bidenate nitrite and chelate nitrate.
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Received: 14 January 2018
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[1] |
Taylor KC. Nitric Oxide Catalysis in Automotive Exhaust Systems[J]. Cheminform, 2010,25(10):457-481.
|
[2] |
Liu L, Yao Z, Liu B, et al. Correlation of structural characteristics with catalytic performance of CuO/CexZr1-xO2catalysts for NO reduction by CO[J]. Journal of Catalysis, 2010,275(1):45-60.
|
[3] |
Iliopoulou E F, Efthimiadis E A, Nalbandian L, et al. Ir-based additives for NO reduction and CO oxidation in the FCC regenerator:Evaluation, characterization and mechanistic studies[J]. Applied Catalysis B:Environmental, 2005,60(3/4):277-288.
|
[4] |
Pérez-Hernández R, Aguilar F, Gómez-Cortés A, et al. NO reduction with CH4or CO on Pt/ZrO2-CeO2catalysts[J]. Catalysis Today, 2005,107-108:175-180.
|
[5] |
屠兢,伏义路,林培琰. Pd/γ-Al2O3三效催化剂中CeO2助剂的作用[J]. 催化学报, 2001,22(4):390-396.
|
[6] |
Holles J H, Davis R J, Murray T M, et al. Effects of Pd particle size and ceria loading on NO reduction with CO[J]. Journal of Catalysis, 2000,195(1):193-206.
|
[7] |
许振冲,吴爽,臧树良. In-Ag/CeO2-γ-Al2O3催化剂上CO-SCR脱除NO的研究[J]. 稀有金属与硬质合金, 2016,44(2):58-63+80.
|
[8] |
Zhu H O, Kim J R, Ihm S K. Selective catalytic reduction of NO with CO on Pt/W-Ce-Zr catalysts[J]. Reaction Kinetics, Mechanisms and Catalysis, 2009,97(2):207-215.
|
[9] |
Wen B, He M. Study of the Cu-Ce synergism for NO reduction with CO in the presence of O, HO and SO in FCC operation[J]. Applied Catalysis B Environmental, 2002,1(37):75-82.
|
[10] |
刘凯杰,于庆波,王奎明,等.低温下CO选择性催化还原NOx的实验研究[J]. 东北大学学报(自然科学版), 2017,38(7):972-977.
|
[11] |
徐春保,吴胜利,苍大强,等. NO-CO-CO2-N2体系中若干金属氧化物对NO去除反应的催化作用[J]. 中国环境科学, 1998,18(3):45-48.
|
[12] |
郭磊,张涛,常化振,等.Ce掺杂改性Ni-Al-Ox催化剂CO-NO反应性能研究[J]. 中国环境科学, https://doi.org/10.19674/j.cnki.issn1000-6923.20180626.001.
|
[13] |
Kantcheva M, Milanova M, Mametsheripov S. In situ FT-IR spectroscopic investigation of gold supported on tungstated zirconia as catalyst for CO-SCR of NOx[J]. Catalysis Today, 2012,191:12-19.
|
[14] |
Qin Y H, Huang L, Zheng J X, et al. Low-temperature selective catalytic reduction of NO with CO over A-Cu-BTC and AOx/CuOy/C catalyst[J]. Inorganic Chemistry Communications, 2016,72:78-82.
|
[15] |
Wang Z, Shen G, Li J, et al. Catalytic removal of benzene over CeO2-MnOx composite oxides prepared by hydrothermal method[J]. Applied Catalysis B Environmental, 2013,138(138):253-259.
|
[16] |
Akram S, Wang Z, Chen L, et al. Low-temperature efficient degradation of ethyl acetate catalyzed by lattice-doped CeO2-CoOx nanocomposites[J]. Catalysis Communications, 2016,73(Supplement C):123-127.
|
[17] |
Damyanova S, Perez C A, Schmal M, et al. Characterization of ceria-coated alumina carrier[J]. Applied Catalysis A:General, 2002, 234(1/2):271-282.
|
[18] |
Fornasiero P, Dimonte R, Rao G R, et al. Rh-Loaded CeO2-ZrO2Solid-Solutions as Highly Efficient Oxygen Exchangers:Dependence of the Reduction Behavior and the Oxygen Storage Capacity on the Structural-Properties[J]. Journal of Catalysis, 1995, 151(1):168-177.
|
[19] |
Tang C, Wang C, Chien S. Characterization of cobalt oxides studied by FT-IR, Raman, TPR and TG-MS[J]. Thermochimica Acta, 2008, 473(1):68-73.
|
[20] |
Liu L, Chen Y, Dong L, et al. Investigation of the NO removal by CO on CuO-CoOx binary metal oxides supported on Ce0.67Zr0.33O2[J]. Applied Catalysis B:Environmental, 2009,90(1):105-114.
|
[21] |
Wang L, W Z C X. In situ DRIFTS study of the NO + CO reaction on Fe-Co binary metal oxides over activated semi-coke supports[J]. RSC Advances, 2017,7(13):7695-7710.
|
[22] |
Dong L, Z B T C. Influence of CeO2 modification on the properties of Fe2O3-Ti0.5Sn0.5O2 catalyst for NO reduction by CO[J]. Catalysis Science & Technology, 2013,4(2):482-493.
|
[23] |
Yao X, Xiong Y, Zou W, et al. Correlation between the physicochemical properties and catalytic performances of CexSn1-xO2 mixed oxides for NO reduction by CO[J]. Applied Catalysis B Environmental, 2014,144(1):152-165.
|
[24] |
Hadjiivanov K. Identification of neutral and charged NxOy surface species by IR spectroscopy[J]. Catalysis Reviews, 2007,42(1& amp;2):71-144.
|
[25] |
Azambre B, Zenboury L, Delacroix F, et al. Adsorption of NO and NO2 on ceria-zirconia of composition Ce0.69Zr0.31O2[J]. Catalysis Today, 2008,137(2-4):278-282.
|
[26] |
Hadjiivanov K, Kn Zinger H. Species formed after NO adsorption and NO+O2co-adsorption on TiO2:an FTIR spectroscopic study[J]. Physical Chemistry Chemical Physics, 2000,2(12):2803-2806.
|
[27] |
Kung M C, Kung H H. IR Studies of NH3, Pyridine, CO, and NO Adsorbed on Transition Metal Oxides[J]. Catalysis Reviews, 1985, 27(3):425-460.
|
|
|
|