| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 60886 | Journal of Catalysis | 2015 | 9 Pages |
•Catalytic effects of physically diluting Pt/NaA and Pt/HA with various acidic metal oxides were studied.•Physical dilution altered the original structure of Pt/NaA due to solid-state H+-exchange.•Physical dilution did not change the structure of decationized form of Pt/NaA (Pt/HA).•Dilution with Al-rich metal oxides can markedly enhance the catalytic activity of Pt/HA.•Lewis acid sites may play a significant role in the catalytic use of hydrogen spillover.
Historically, Pt/LTA (e.g., Pt/NaA) has often been used as a model catalyst for studying the catalytic functions of hydrogen spillover (H spillover). Notably, none of the works reported appreciable catalytic activities for Pt/LTA alone, while markedly enhanced activities were reported after physical dilution with some acidic oxides. It was often speculated without experimental evidence that activated hydrogen generated from Pt/LTA can migrate to the diluents surface (“inter-particular” H spillover) where organic reactants can react with spilt-over hydrogen. In this work, we carefully studied benzene hydrogenation activities of Pt/NaA and its decationized form (Pt/HA), before and after the physical dilution with various metal oxides possessing different Lewis and Brønsted acidity. The originally negligible activity of Pt/NaA increased significantly after mixing with various acidic oxides. The physical dilutions, however, resulted in a significant alteration of Pt/NaA structure due to solid-state H+ exchange, which made the catalytic interpretation vague. In contrast, Pt/HA structure did not change after the dilutions, and thus could be used as an ideal catalytic model system for studying inter-particular H spillover. The catalytic results showed that Al-rich metal oxides with abundant Lewis acid sites are effective for enhancing the catalytic activity.
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