Elaboration and characterization of sulfated and unsulfated V2O5/TiO2 nanotubes catalysts for chlorobenzene total oxidation

被引:74
作者
Gannoun, C. [1 ]
Turki, A. [1 ]
Kochkar, H. [1 ,2 ]
Delaigle, R. [3 ]
Eloy, P. [3 ]
Ghorbel, A. [1 ]
Gaigneaux, E. M. [3 ]
机构
[1] Fac Sci Tunis, Lab Chim Mat & Catalyse, El Manar 2092, Tunisia
[2] Ctr Natl Rech Sci Mat, Technopole Borj Cedria, Hammam Lif 2050, Tunisia
[3] Catholic Univ Louvain, Div Solids Mol & React MOST, Inst Condensed Matter & Nanosci IMCN, B-1348 Louvain, Belgium
关键词
TiO2; nanotubes; Sulfate; Vanadia; Chlorobenzene oxidation; SUPPORTED VANADIA CATALYSTS; OXIDE-BASED FORMULATIONS; TITANATE NANOTUBES; CALCINATION TEMPERATURE; REDUCTION; NO; NH3; ACID; 1,2-DICHLOROBENZENE; BEHAVIOR;
D O I
10.1016/j.apcatb.2013.08.009
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
This paper examines the use of TiO2 nanotubes (HNTs) as supports for V2O5 based catalysts in the total oxidation of chlorobenzene. The effect of the addition of SO42- onto the support is also discussed. Vanadium was introduced either by direct incorporation of V during the elaboration of the nanotubes (in situ elaboration), or by the impregnation of V on the surface of the supports (ex situ elaboration). The obtained catalysts have been characterized by means of ICP-AES, N-2 adsorption-desorption at 77K, XRD, DRIFTS, XPS, H-2-TPR and NH3-TPD. We demonstrated that sulfating step highly improves the catalytic performances of V-HNTs catalysts. This is due to an increased global acidity and a higher reactivity of redox sites thanks to the electronic interaction between sulfated titania and VOx species. Moreover, it seems that the 'in situ' or 'ex situ' elaboration route of sulfated V-catalysts influences the environment of vanadium species. In particular, the 'in situ' route leads to a more efficient catalyst. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:58 / 64
页数:7
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