钼酸盐
催化作用
X射线吸收光谱法
拉曼光谱
甲醇
化学
无机化学
吸收光谱法
材料科学
核化学
有机化学
量子力学
光学
物理
作者
Abhijeet Gaur,Max Schumann,Kristian Viegaard Raun,M. Stehle,Pablo Beato,Anker Degn Jensen,Jan‐Dierk Grunwaldt,Martin Høj
出处
期刊:Chemcatchem
[Wiley]
日期:2019-07-15
卷期号:11 (19): 4871-4883
被引量:31
标识
DOI:10.1002/cctc.201901025
摘要
The structural changes of an iron molybdate/molybdenum oxide (Mo/Fe=2.0) catalyst for the selective oxidation of methanol to formaldehyde were studied using combined operando X‐ray absorption spectroscopy (XAS) and X‐ray diffraction (XRD) as well as operando Raman spectroscopy. Under operating conditions, the Mo K‐edge XANES spectra showed a transition from a mixture of α‐MoO3 and Fe2(MoO4)3 towards only Fe2(MoO4)3. XRD and Raman spectroscopy also showed disappearance of the α‐MoO3 phase with time on stream. The results evidenced that the α‐MoO3 component evaporated completely, while the Fe2(MoO4)3 component remained stable. This was linked to a decrease in catalytic activity. Further studies unraveled that the rate of α‐MoO3 evaporation increased with increasing MeOH concentration, decreasing O2 concentration and increasing temperature. The simultaneous measurements of catalytic activity and spectroscopy allowed to derive a structure‐activity relationship showing that α‐MoO3 evaporation needs to be prevented to optimize MoO3‐based catalysts for selective oxidation of methanol.
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