In situ studies of surface of NiFe2O4 catalyst during complete oxidation of methane

被引:36
作者
Zhang, Shiran [1 ,2 ]
Shan, Junjun [1 ,2 ]
Nie, Longhui [3 ]
Luan Nguyen [1 ,2 ]
Wu, Zili [4 ,5 ]
Tao, Franklin [1 ,2 ]
机构
[1] Univ Kansas, Dept Chem & Petr Engn, Lawrence, KS 66045 USA
[2] Univ Kansas, Dept Chem, Lawrence, KS 66045 USA
[3] Hubei Univ Technol, Sch Chem & Chem Engn, Wuhan 430068, Peoples R China
[4] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
[5] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
complete oxidation; transition metal oxide; methane; In situ study; NANOCRYSTALLINE SPINEL NIFE2O4; WATER-GAS SHIFT; LOW-TEMPERATURE; PARTICLE-SIZE; CH4; OXIDATION; PD CATALYSTS; METAL; PALLADIUM; COMBUSTION; CHEMISTRY;
D O I
10.1016/j.susc.2015.12.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
NiFe2O4 with an inverse spinel structure exhibits high activity for a complete oxidation of methane at 400 degrees C-425 degrees C and a higher temperature. The surface of the catalyst and its adsorbates were well characterized with ambient pressure X-ray photoelectron spectroscopy (AP-XPS) and in situ infrared spectroscopy (IR). In situ studies of the surface of NiFe2O4 using AP-XPS suggest the formation of methoxy-like and formate-like intermediates at a temperature lower than 200 degrees C, supported by the observed vibrational signatures in in situ IR studies. Evolutions of C1s photoemission features and the nominal atomic ratios of C/(Ni + Fe) of the catalyst surface suggest that the formate-like intermediate is transformed to product molecules CO2 and H2O in the temperature range of 250-300 degrees C. In situ studies suggest the formation of a spectator,-O-lattice-CH2-O-lattice-. It strongly bonds to surface through C-O bonds and cannot be activated even at 400 degrees C. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:156 / 162
页数:7
相关论文
共 50 条
[1]  
Andrushkevich T.B.. G., 1968, KINET KATAL, V9, P1244
[2]  
Andrushkevich T.B..G., 1968, KINET KATAL, V9, P595
[3]   OXIDATION OF PROPENE ON MIXED OXIDES OF COPPER AND COBALT [J].
BAUSSART, H ;
DELOBEL, R ;
LEBRAS, M ;
LEROY, JM .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1979, 75 :1337-1345
[4]   FT-IR STUDY OF THE ADSORPTION AND TRANSFORMATION OF FORMALDEHYDE ON OXIDE SURFACES [J].
BUSCA, G ;
LAMOTTE, J ;
LAVALLEY, JC ;
LORENZELLI, V .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (17) :5197-5202
[5]  
Cargnello M, 2012, SCIENCE, V337, P713, DOI [10.1126/science.1223488, 10.1126/science.1222887]
[6]   Consequences of Metal-Oxide Interconversion for C-H Bond Activation during CH4 Reactions on Pd Catalysts [J].
Chin, Ya-Huei ;
Buda, Comeliu ;
Neurock, Matthew ;
Iglesia, Enrique .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (41) :15425-15442
[7]   Low-Temperature Oxidation of Methane [J].
Farrauto, Robert J. .
SCIENCE, 2012, 337 (6095) :659-660
[8]   Complete oxidation of methane at low temperature over Pt and Pd catalysts for the abatement of lean-burn natural gas fuelled vehicles emissions:: influence of water and sulphur containing compounds [J].
Gélin, P ;
Urfels, L ;
Primet, M ;
Tena, E .
CATALYSIS TODAY, 2003, 83 (1-4) :45-57
[9]   Complete oxidation of methane at low temperature over noble metal based catalysts:: a review [J].
Gélin, P ;
Primet, M .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2002, 39 (01) :1-37
[10]   Activity of PdO/SiO2 catalysts for CH4 oxidation following thermal treatments [J].
Gholami, Rahman ;
Smith, Kevin J. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2015, 168 :156-163