Ultrafine rare earth molybdenum (La-Mo and Ce-Mo) complex oxide particles have been synthesized by the sol-gel process using citric acid as complexing agent. The influence of preparation conditions such as thermal treatment temperature (T), molar ratio of citric acid to metallic ions (L/M), and pH v
Laser Raman and XPS analyses of molybdenum–rare earth oxide catalysts
✍ Scribed by J. M. López Nieto; V. Cortés Corberán; J. L. G. Fierro
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 667 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0142-2421
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Laser Raman spectroscopy (LRS) and x‐ray photoelectron spectroscopy (XPS), combined with x‐ray diffraction (XRD), have been used to characterize the phases in Mo–RE–O (RE = Sm, Tb, Yb) systems. Two clearly differentiated composition regions were observed, namely the RE‐rich region (x < 0.5–0.6, where x represents the Mo/(Mo + RE) atomic ratio), in which the RE oxide was always present as a separate phase, and the Mo‐rich region (x > 0.6) in which MoO~3~ appeared as a separate phase. The broadening of the Raman bands in the RE‐rich region is indicative of the presence of ill‐defined structures. However, as the RE oxide content increased, crystalline molybdates with decreasing Mo/RE ratios were found in each system. XPS surface composition was roughly similar to that of the bulk for the Mo–Sm–O and Mo–Yb–O series, while relevance of MoO~3~ and molybdate phases in the Mo‐rich composition regions is discussed in the context of allylic oxidation of light olefins.
📜 SIMILAR VOLUMES
## Abstract Neodymium tris(2‐ethylhexylphosphonate)‐triisobutylaluminum‐water system was investigated as a catalyst in ethylene oxide and propylene oxide copolymerization. Random copolymers of ethylene oxide and propylene oxide were obtained with high yield and high molecular weight in a short reac
## Sr-promoted rare earth (viz. La, Ce, Pr, Nd, Sm, Eu, Gd, Dy, Er and Yb) oxide catalysts (Sr/rare earth ratio \ 0É1) are compared for their performance in the oxidative coupling of methane (OCM) to hydrocarbons and C 2 oxidative dehydrogenation of ethane (ODE) to ethylene at di †erent temperatur