VOx species on alumina at high vanadia loadings and calcination temperature and their role in the ODP reaction

被引:58
作者
Steinfeldt, N [1 ]
Müller, D [1 ]
Berndt, H [1 ]
机构
[1] Inst Appl Chem, D-12489 Berlin, Germany
关键词
oxidative dehydrogenation; propane; vanadia; alumina; NMR; TPR; ESR; UV-vis;
D O I
10.1016/j.apcata.2004.05.050
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
Vanadium species formed on the alumina support after calcination between 773 and 973 K at vanadium loadings between 4.45 and 13.2 wt.% were characterized with different methods (V-51 NMR, ESR, H-2-TPR and in situ UV-vis-DRS) and tested in the oxidative dehydrogenation of propane. By calcination at 873 K, beside dispersed isolated and polymerized V5+ surface species mainly in tetrahedral coordination, a crystalline AIVO(4) phase was formed. The portion of vanadium present as AIVO(4) increases with increasing vanadium loadings (e.g. about 60 at 13.2 wt.%). The domain size of the polymerized V5+ species is only weakly influenced by the vanadium loadings at calcination up to 873 K. It is suggested that both isolated and polymerized tetrahedrally coordinated V5+ species are active in propane dehydrogenation. The AIVO(4) phase and bulk-like V2O5 have only a low catalytic activity. The highest propene selectivity was obtained for the sample with the highest dispersion of the isolated and polymerized tetrahedrally coordinated V5+ species. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:201 / 213
页数:13
相关论文
共 39 条
[1]  
[Anonymous], 2014, SYNTHESIS CHARACTERI
[2]   Structure and dispersion of supported-vanadia catalysts. Influence of the oxide carrier [J].
Arena, F ;
Frusteri, F ;
Parmaliana, A .
APPLIED CATALYSIS A-GENERAL, 1999, 176 (02) :189-199
[3]   Surface structures, reduction pattern and oxygen chemisorption of V2O5/SiO2 catalysts [J].
Arena, F ;
Frusteri, F ;
Martra, G ;
Coluccia, S ;
Parmaliana, A .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1997, 93 (21) :3849-3854
[4]   Effect of catalyst structure on oxidative dehydrogenation of ethane and propane on alumina-supported vanadia [J].
Argyle, MD ;
Chen, KD ;
Bell, AT ;
Iglesia, E .
JOURNAL OF CATALYSIS, 2002, 208 (01) :139-149
[5]   STRUCTURE OF MONOLAYER TYPE VANADIUM PENTOXIDE, SUPPORTED ON GAMMA-ALUMINA [J].
BERGERET, G ;
GALLEZOT, P ;
CHARY, KVR ;
RAO, BR ;
SUBRAHMANYAM, VS .
APPLIED CATALYSIS, 1988, 40 (1-2) :191-196
[6]   Structure and catalytic properties of VOx/MCM materials for the partial oxidation of methane to formaldehyde [J].
Berndt, H ;
Martin, A ;
Brückner, A ;
Schreier, E ;
Müller, D ;
Kosslick, H ;
Wolf, GU ;
Lücke, B .
JOURNAL OF CATALYSIS, 2000, 191 (02) :384-400
[7]   Oxidative dehydrogenation of ethane and n-butane on VOx/Al2O3 catalysts [J].
Blasco, T ;
Galli, A ;
Nieto, JML ;
Trifiro, F .
JOURNAL OF CATALYSIS, 1997, 169 (01) :203-211
[8]   Oxidative dehydrogenation of short chain alkanes on supported vanadium oxide catalysts [J].
Blasco, T ;
Nieto, JML .
APPLIED CATALYSIS A-GENERAL, 1997, 157 (1-2) :117-142
[9]   FACTORS INFLUENCING THE TEMPERATURE-PROGRAMMED REDUCTION PROFILES OF VANADIUM PENTOXIDE [J].
BOSCH, H ;
KIP, BJ ;
VANOMMEN, JG ;
GELLINGS, PJ .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1984, 80 :2479-2488
[10]   CHEMICAL AND SPECTROSCOPIC STUDY OF THE NATURE OF A VANADIUM-OXIDE MONOLAYER SUPPORTED ON A HIGH-SURFACE-AREA TIO2 ANATASE [J].
BUSCA, G ;
CENTI, G ;
MARCHETTI, L ;
TRIFIRO, F .
LANGMUIR, 1986, 2 (05) :568-577