The influence of nonstoichiometry on LaMnO3 perovskite for catalytic NO oxidation

被引:215
作者
Chen, Jiahao [1 ]
Shen, Meiqing [1 ,2 ]
Wang, Xinquan [1 ]
Qi, Gongshin [3 ]
Wang, Jun [1 ]
Li, Wei [3 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, State Educ Minist, Tianjin 300072, Peoples R China
[2] Tianjin Univ, State Key Lab Engines, Tianjin 300072, Peoples R China
[3] Gen Motors Global Res & Dev, Chem Sci & Mat Syst Lab, Warren, MI 48090 USA
来源
APPLIED CATALYSIS B-ENVIRONMENTAL | 2013年 / 134卷
基金
国家高技术研究发展计划(863计划);
关键词
NO oxidation; Mn4+/Mn3+ ratio; Nonstoichiometry; LaMnO3; perovskite; METHANE COMBUSTION; STRUCTURAL DEFECTS; CO; LANTHANUM; STORAGE; REDUCTION; PLATINUM; SR; SUBSTITUTION; PERFORMANCE;
D O I
10.1016/j.apcatb.2013.01.027
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
A series of structural modified LaxMnO3 (x = 0.9, 0.95, 1, 1.05, 1.11) perovskites used for NO oxidation was synthesized by a sol-gel method and characterized by XRD, BET, XPS, EPR and H-2-TPR. La0.9MnO3 sample exhibits superior activity, and a 50% NO conversion at 250 degrees C is obtained. XPS and EPR results reveal a higher Mn4+/Mn3+ ratio in Mn-rich samples, which induce more active oxygen bonding to Mn4+ due to the need for balancing the chemical states and stabilizing the structure. Easily regenerated oxygen associated with Mn4+ catalyzes the low-temperature NO oxidation. The constant activation energy (44.8 kJ/mol) obtained in the kinetics tests indicates the same mechanism of NO oxidation operated on all the samples. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:251 / 257
页数:7
相关论文
共 49 条
[1]
Ahranjani R.E., 2011, CHEM ENG J, V169, P282
[2]
Photocatalysis with nanostructured zinc oxide thin films: The relationship between morphology and photocatalytic activity under oxygen limited and oxygen rich conditions and evidence for a Mars Van Krevelen mechanism [J].
Ali, Arshid M. ;
Emanuelsson, Emma A. C. ;
Patterson, Darrell A. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2010, 97 (1-2) :168-181
[3]
Non-stoichiometry, structural defects and properties of LaMnO3+delta with high delta values (0.1<=delta<=0.29) [J].
Alonso, JA ;
MartinezLope, MJ ;
Casais, MT ;
MacManusDriscoll, JL ;
deSilva, PSIPN ;
Cohen, LF ;
FernandezDiaz, MT .
JOURNAL OF MATERIALS CHEMISTRY, 1997, 7 (10) :2139-2144
[4]
Structuration of LaMnO3 perovskite catalysts on ceramic and metallic monoliths:: Physico-chemical characterisation and catalytic activity in methane combustion [J].
Arendt, E. ;
Maione, A. ;
Klisinska, A. ;
Sanz, O. ;
Montes, M. ;
Suarez, S. ;
Blanco, J. ;
Ruiz, P. .
APPLIED CATALYSIS A-GENERAL, 2008, 339 (01) :1-14
[5]
The effect gas composition during thermal aging on the dispersion and NO oxidation activity over Pt/Al2O3 catalysts [J].
Auvray, Xavier ;
Pingel, Torben ;
Olsson, Eva ;
Olsson, Louise .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2013, 129 :517-527
[6]
Azad H.Z., 2011, APPL CATAL B-ENVIRON, V102, P62
[7]
Rapid synthesis of room temperature ferromagnetic Ag-doped LaMnO3 perovskite phases by the solution combustion method [J].
Bellakki, Manjunath B. ;
Shivakumara, C. ;
Vasanthacharya, N. Y. ;
Prakash, A. S. .
MATERIALS RESEARCH BULLETIN, 2010, 45 (11) :1685-1691
[8]
Structure-activity relationships of Pt/Al2O3 catalysts for CO and NO oxidation at diesel exhaust conditions [J].
Boubnov, Alexey ;
Dahl, Soren ;
Johnson, Erik ;
Molina, Anna Puig ;
Simonsen, Soren Bredmose ;
Cano, Fernando Morales ;
Helveg, Stig ;
Lemus-Yegres, Lived J. ;
Grunwaldt, Jan-Dierk .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2012, 126 :315-325
[9]
Kinetic experiments and modeling of NO oxidation and SCR of NOx with decane over Cu- and Fe-MFI catalysts [J].
Capek, Libor ;
Vradman, Leonid ;
Sazama, Petr ;
Herskowitz, Moti ;
Wichterlova, Blanka ;
Zukerman, Roie ;
Brosius, Roald ;
Martens, Johan A. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2007, 70 (1-4) :53-57
[10]
Methane combustion and CO oxidation on LaAl1-xMnxO3 perovskite-type oxide solid solutions [J].
Cimino, S ;
Lisi, L ;
De Rossi, S ;
Faticanti, M ;
Porta, P .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 43 (04) :397-406