Structural characterisation of silica supported CoMo catalysts by UV Raman spectroscopy, XPS and X-ray diffraction techniques

被引:67
作者
La Parola, V
Deganello, G
Tewell, CR
Venezia, AM
机构
[1] Univ Palermo, Dipartimento Chim Inorgan Chim Anal S Cannizzoro, I-90128 Palermo, Italy
[2] CNR, Inst Studio Mat Nanostrutturai, Sez Palermo, I-90146 Palermo, Italy
[3] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
关键词
CoMo/silica; HDS; sodium; Raman; XPS;
D O I
10.1016/S0926-860X(02)00261-2
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 structure of Co-Mo catalysts supported on commercial silica, doped with various amounts of sodium ions, was investigated by means of X-ray diffraction (XRD), UV-Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). Two series of samples were considered. One series was prepared by classic incipient wet impregnation (WI) and the other series by co-impregnation in the presence of nitrilotri acetic acid (NTA). The effect of sodium on the catalyst structure depended on the preparation procedure: in the case of the WI catalysts, sodium promoted the transformation of the polymolybdate species into monomolybdate Na2MoO4; in the case of the NTA prepared samples, sodium induced transformation from heptamolybdates, Mo2O72- and mixed CoMo oxides into MoO42- units with distorted tetrahedral symmetry without forming Na2MoO4 compound. In addition to purely structural modifications, sodium induced an electronic effect, evidenced by Mo 3d and Co 2p XPS binding energy shifts. The catalytic behaviour of the samples, previously tested in the HDS of thiophene, was explained in terms of structural and electronic changes. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:171 / 180
页数:10
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