Time-of-flight SIMS study of heterogeneous catalysts based on praseodymium and molybdenum oxides

被引:35
作者
De Smet, F
Devillers, M
Poleunis, C
Bertrand, P
机构
[1] Univ Catholique Louvain, Lab Chim Inorgan & Analyt, B-1348 Louvain, Belgium
[2] Univ Catholique Louvain, Unite Physicochim & Phys Mat, B-1348 Louvain, Belgium
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1998年 / 94卷 / 07期
关键词
D O I
10.1039/a707883h
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 [物理化学]; 081704 [应用化学];
摘要
Time-of-flight secondary ion mass spectrometry (TOF SIMS) analyses have been performed on MoO3-Pr6O11 mixtures before and after their use in the selective oxidation of isobutene to methacrolein at 673 K. The three pure molybdate phases (Pr2MoO6, Pr2Mo3O12, Pr6MoO12) obtained independently by the citrate route have also been examined to determine their respective SIMS fragmentation patterns. Although the Pr2MoO6 and Pr2Mo3O12 phases were found to give the same molecular fragments, these phases could be distinguished by the relative intensity ratios of some particular species. Identification of Pr6MoO12 was easier owing to the presence of characteristic high-mass mixed Pr-Mo fragments. A linear relationship was observed when plotting the experimental intensity ratios of several molecular fragments against the Pr/Mo bulk composition. The same behaviour was also noticed for a series of Pr6O11-MoO3 mixtures. Moreover, the examination of the 3-D crystal structure of the pure molybdate phases indicates that the fragmentation patterns of these phases were directly related to their structure. As far as the used catalysts were concerned, the SIMS results showed that: (i) the experimental intensity ratios of given fragments were much smaller in the used catalysts than in the fresh ones; (ii) fragments characteristic of the Pr6MoO12 phase were absent; and (iii) differences in the relative SIMS intensities of certain fragments showed the dominant presence of the Pr2Mo3O12 phase.
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页码:941 / 947
页数:7
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