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Ethanol Conversion to Ethylene and Acetaldehyde over Rhodium(I) Exchanged Faujasite Zeolite. A QM/MM and Microkinetic Study

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posted on 25.01.2018, 16:00 by Velina Markova, Graham Rugg, Agalya Govindasamy, Alexander Genest, Notker Rösch
In a computational study, we examined the conversion of ethanol to ethylene or acetaldehyde over Rh­(I)-exchanged zeolite (faujasite) using QM/MM DFT calculations and microkinetic modeling. To elucidate how the composition of the active site affects the reactivity in this model system, the dehydration and dehydrogenation reaction mechanisms at the Rh center were modeled by varying the number n (n = 1–3) of preadsorbed ethanol molecules. For a coverage of one ethanol, ethylene formation was determined to proceed via a two-step mechanism, whereas concerted C­(β)-H and C–O bond cleavage occurs for higher coverage at the metal center. In contrast, the dehydrogenation mechanism of ethanol does not vary with coverage. A crucial step in both transformations is the expulsion of the products which was found to be more facile at higher ethanol coverage, n = 2, 3. However, at n = 1, we calculated much lower barriers for the corresponding bond scission steps. Microkinetic modeling, based on the QM/MM results, revealed a strong temperature dependence of the activity of the catalytic system. Little to no reactivity is predicted at lower temperatures, whereas both types of reactions appear likely at temperatures above 500 K. Up to 700 K, the accumulated amount of acetaldehyde is higher than that of ethylene. At even higher temperatures ethylene is predicted as the preferred product.

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