Abstract
Converting high-performing powder catalysts from the laboratory reactor scale into effective extruded catalysts at the industrial scale remains a hurdle for advancing sustainable catalytic processes, such as the conversion of biogenic syngas into high octane gasoline. Recently, a process-intensified syngas-to-hydrocarbons (STH) reaction in a single reactor under relatively mild conditions (220-250 degrees C, 0.75-2.0?MPa) was reported, enabled by the development of a dimethyl ether (DME) homologation catalyst, Cu-modified H-BEA (Cu/BEA) zeolite. In this study, we explore approaches for synthesizing engineered Cu/BEA catalysts for use in the STH reaction to retain the high performance observed with the powder catalyst. We demonstrate that changes to the order of manufacturing steps (i.e., Cu deposition, alumina binder addition, and extrusion) result in observable changes to key active sites (Bronsted acid sites and zeolitic Cu+ species), and ultimately, catalyst performance. When the Cu precursor was added directly to BEA before extrusion, both types of active sites were stabilized, preserving the activity of the powder catalyst. However, when the Cu precursor was added after extrusion, the resulting Cu species were mobile, destabilizing Bronsted acid sites and leading to near-zero activity.
| Original language | American English |
|---|---|
| Number of pages | 14 |
| Journal | Applied Catalysis B: Environmental |
| Volume | 387 |
| DOIs | |
| State | Published - 2026 |
NLR Publication Number
- NLR/JA-5100-97193
Keywords
- engineered catalysts
- extrusion
- syngas to hydrocarbons
- synthetic fuels
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