Complementary operando insights into the activation of multicomponent selective propylene oxidation catalysts
M. Stehle, Abhijeet Gaur, Sebastian Weber, Thomas L. Sheppard, Michael Thomann, Achim Fischer, Jan‐Dierk Grunwaldt
Abstract
Two Bi–Mo–Co–Fe–O catalysts were synthesized by flame spray pyrolysis and tested for their catalytic performance in selective oxidation of propylene to acrolein. Pronounced structural changes during temperature–programmed oxidation and reaction were observed by operando X–ray absorption spectroscopy, X–ray diffraction, Raman spectroscopy, and thermogravimetric analysis. During oxidative treatment, mainly binary oxide phases (α–Bi2Mo3O12, β–CoMoO4, Fe2(MoO4)3) were observed, but single (MoO3) or ternary (Bi3(FeO4)(MoO4)2) oxides also formed depending on the relative elemental catalyst composition. During propylene oxidation, the reduction of Fe3+ to Fe2+ led to a strong rise in activity and induced further phase transformations. MoO3 was found to be unselective towards acrolein but was essential in binding other single oxides. The formation of β–Co0.7Fe0.3MoO4 and Bi3(FeO4)(MoO4)2 as well as their synergistic interplay with α–Bi2Mo3O12 are key factors for high performance. The combination of complementary operando methods was crucial to reveal new structure–activity/selectivity correlations, therefore bridging the knowledge gap between simplified model systems and complex applied catalysts.