Surface and structural properties of zirconia-supported vanadium oxide influence of the preparation pH

被引:6
|
作者
Valigi, M
Gazzoli, D
Ferraris, G
De Rossi, S
Spinicci, R
机构
[1] Univ Roma La Sapienza, CNR, IMIP, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, Dipartimento Chim, IMIP, I-00185 Rome, Italy
[3] Univ Florence, Dipartimento Energet, I-50139 Florence, Italy
关键词
D O I
10.1016/j.molcata.2004.10.007
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
Zirconia-supported vanadium oxide catalysts were prepared by equilibrium adsorption in acid (pH 2.7) or basic (pH 10) conditions using hydrous zirconium oxide and an aqueous solution of ammonium metavanadate. The samples, containing vanadium up to 22.24 wt.%, heated at 823 K for 5 h in air. were studied as prepared and after leaching with an ammonia solution by X-ray diffraction, X-ray photoelectron spectroscopy, diffuse optical reflectance, surface area measurements and pore size distribution determination. Owing to the microporous support and to the different condensation degree of the vanadium species, the precursors showed distinct features. The diversity persisted after heating and became more evident at increasing vanadium content. At similar vanadium loading, the fraction in a dispersed state and thus interacting with the support was higher in samples at pH 10 than in those prepared at pH 2.7. For pH 2.7 samples, heating favoured the formation Of V2O5 and of ZrV2O7. The interaction between the vanadium dispersed species and the zirconia surface strongly affected the texture. sintering and phase transition of the support. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 66
页数:8
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