Amorphous features of working catalysts:: XAFS and XPS characterization of Mn/Na2WO4/SiO2 as used for the oxidative coupling of methane

被引:77
作者
Kou, Y
Zhang, B
Niu, JZ
Li, SB
Wang, HL
Tanaka, T
Yoshida, S
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] Kyoto Univ, Dept Mol Engn, Kyoto 60601, Japan
关键词
D O I
10.1006/jcat.1997.1900
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
Mn/Na2WO4/SiO2 catalyst for the oxidative coupling of methane has been investigated by using the L-edge and the K-edge XAFS and XPS, The surface of the fresh catalyst is found to be dominated by oxygen-enriched amorphous phases consisting of discretely distributed tetrahedral WO4 and octahedral MnO6 groups, The average bond lengths, which is 1.77 Angstrom for W-O and 2.00 Angstrom for Mn-O, are fully identical to those in pure Na2WO4 and Mn2O3. However, on the used catalyst after a 450 h run, almost no tungsten species is detectable. Instead, tetrahedral manganese sites are observed, The surface of the used catalyst is dominated by highly dispersed MnO4 groups consisting of tetrahedral and coordinatively unsaturated octahedral sites. The average Mn-O bond length increases to 2.09 Angstrom while the Mn 2P(3/2) binding energy increases from 641.4 eV (Mn3+) to 641.7 eV (Mn2+), These results suggest that the combination of tetrahedral and octahedral metallic cores with different oxidation states from each other is responsible for the catalysis in the oxidative coupling of methane, and that the high activity of the manganese-tungsten catalyst is due to the surface oxygen species, which are pre-activated from lattice oxygens to "the nearest oxygens" by the surface in an amorphous state. (C) 1998 Academic Press.
引用
收藏
页码:399 / 408
页数:10
相关论文
共 42 条
[1]   The oxidative coupling of methane over BaCO3/LaOBr-catalysts of high ethylene yield [J].
Au, CT ;
He, H ;
Lai, SY ;
Ng, CF .
JOURNAL OF CATALYSIS, 1996, 163 (02) :399-408
[2]   X-RAY-ABSORPTION NEAR-EDGE STRUCTURE OF 3D TRANSITION-ELEMENTS IN TETRAHEDRAL COORDINATION - THE EFFECT OF BOND-LENGTH VARIATION [J].
BIANCONI, A ;
FRITSCH, E ;
CALAS, G ;
PETIAU, J .
PHYSICAL REVIEW B, 1985, 32 (06) :4292-4295
[3]  
BIANCONI A, 1988, TOP CURR CHEM, V145, P29
[4]   ANION BINDING TO BOVINE ERYTHROCYTE SUPEROXIDE-DISMUTASE STUDIED BY X-RAY ABSORPTION-SPECTROSCOPY - A DETAILED STRUCTURAL-ANALYSIS OF THE NATIVE ENZYME AND THE AZIDO AND CYANO DERIVATIVES USING A MULTIPLE-SCATTERING APPROACH [J].
BLACKBURN, NJ ;
STRANGE, RW ;
MCFADDEN, LM ;
HASNAIN, SS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (23) :7162-7170
[5]   STAGES IN THE MODIFICATION OF A SILVER SURFACE FOR CATALYSIS OF THE PARTIAL OXIDATION OF ETHYLENE [J].
BUKHTIYAROV, VI ;
BORONIN, AI ;
SAVCHENKO, VI .
JOURNAL OF CATALYSIS, 1994, 150 (02) :262-267
[6]  
BUKHTIYAROV VI, 1994, J CATAL, V150, P268, DOI 10.1006/jcat.1994.1345
[7]  
CHRIST CL, 1989, DESCRIPTIVE CRYSTAL
[8]   OXIDATION-STATE ASSIGNMENTS FOR GALACTOSE-OXIDASE COMPLEXES FROM X-RAY ABSORPTION-SPECTROSCOPY - EVIDENCE FOR CU(II) IN THE ACTIVE ENZYME [J].
CLARK, K ;
PENNERHAHN, JE ;
WHITTAKER, MM ;
WHITTAKER, JW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (17) :6433-6434
[9]  
COTTON FA, 1980, ADV INORG CHEM, P850
[10]  
Cox A.D., 1981, EXAFS INORGANIC SYST, P51