Abstract
Redox and photo‐redox properties of isolated Mo5+ ions stabilized in H‐ZSM‐5 and H‐beta zeolites are studied by in situ ESR in flowing O2, NO, H2, and C3H6. Upon oxidation of pre‐reduced samples at 20 °C, NO demonstrates a higher oxidative ability, as compared with O2. Interaction of Mo5+ ions with propene at 20 °C results in formation of a chemisorption complex with enhanced reactivity of Mo(V) toward NO. Illumination of the Mo5+/HZSM‐5 sample with UV‐visible light causes measurable acceleration of Mo(V) oxidation by NO at 20 °C. Therefore, photochemical activation of the oxidation step could be realized, in principle, for Mo/zeolite catalysts. At 500 °C in the reaction mixture NO + H2, the step of the catalytic site reduction is fast, and the dynamic equilibrium of the redox reaction Mo(VI) ↔ Mo(V) for MoH‐ZSM‐5 and MoH‐beta seems to be strongly shifted to Mo5+.
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