Vanadium phosphorus oxide catalyst modified by niobium doping for mild oxidation of n-butane to maleic anhydride

被引:51
作者
de Farias, AMD
Gonzalez, WD
de Oliveira, PGP
Eon, JG
Herrmann, JM
Aouine, M
Loridant, S
Volta, JC
机构
[1] Inst Rech Catalyse, F-69626 Villeurbanne, France
[2] Inst Militar Engn, Rio De Janeiro, Brazil
[3] Inst Nacl Tecnol, Lab Catalise, Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro, Inst Quim, Rio De Janeiro, Brazil
[5] Ecole Cent Lyon, Lab Photocatalyse Catalyse & Environm, IFOS, F-69131 Ecully, France
关键词
n-butane mild oxidation; maleic anhydride; vanadium phosphorus oxide; niobium doping;
D O I
10.1006/jcat.2002.3562
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
The interest of doping (VO)(2)P2O7 with Nb5+ ions has been studied for n-butane oxidation to maleic anhydride. Nb was solubilized as niobium (V) ethoxide into isobutanol and used as a reducing reagent to prepare the VOHPO4 . 0.5H(2)O precursor. Under n-butane fuel-lean oxidation conditions, the VNbPO precursor was activated at a temperature 20degreesC lower than for undoped VPO because of a modification of its morphology. Electron microscopy showed that the activated VNbPO catalyst is more disorganized than the activated VPO. It contains more defects and concentrates Nb at the surface. Nb acts as an n-type dopant for the p-type (VO)(2)P2O7 semiconductor, as observed in electrical conductivity measurements. P-31 NMR by spin-echo mapping and XPS spectroscopy provide evidence that the VNbPO catalyst is more oxidized, particularly at the surface. Doping with Nb creates defects, responsible for C-H n-butane activation, which have been observed to be associated with Lewis acid sites of low acidity. This is the reason for the enhancement of the n-butane conversion. Selectivity to maleic anhydride is not modified by Nb-doping while CO2/CO formation is increased due to the higher surface V5+/V4+ ratio. (C) 2002 Elsevier Science (USA).
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页码:238 / 246
页数:9
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