Issue 29, 2024

Design of novel hierarchical cage active particles and zeolite for the direct conversion of syngas to gasoline fuel

Abstract

Although the direct conversion of syngas to gasoline fuel offers a promising route to produce liquid fuel from non-petroleum carbon resources, it remains a great challenge owing to low target product selectivity and poor catalyst stability. Hence, we designed a bifunctional catalyst consisting of SiO2-coated novel hierarchical porous cage active particles and hierarchical porous zeolite, which provided a C5–C11 hydrocarbon selectivity of 63.5 wt%, and the yield reached 99.3% in C5+ hydrocarbons, with an aromatic content of 25.7% at 280 °C. Particularly, this value is within the range of the restricted aromatic content. As the reaction temperature was elevated to 310 °C, zeolite-24 presented an excellent aromatic selectivity of 64.4% in liquid hydrocarbons. This is mainly because the zeolite provides higher acidity at a rather high reaction temperature, facilitating the formation of hydrocarbons in the liquid phase, which were predominantly aromatics rather than i-C5+. Besides aromatics, a high i-C5+ content of 77.4% in liquid hydrocarbons was obtained at 280 °C over FeZ-16. At the given condition, the synthesized hybrid catalysts were beneficial for the production of gasoline fuels consisting of aromatics and i-C5+. Particularly, 280 °C offered optimum selectivity to i-C5+, and 310 °C was suitable for the formation of aromatics. This work provides a strategy for the design and preparation of novel and efficient catalysts for gasoline production.

Graphical abstract: Design of novel hierarchical cage active particles and zeolite for the direct conversion of syngas to gasoline fuel

Supplementary files

Article information

Article type
Paper
Submitted
26 Feb 2024
Accepted
25 Jun 2024
First published
25 Jun 2024

New J. Chem., 2024,48, 13000-13009

Design of novel hierarchical cage active particles and zeolite for the direct conversion of syngas to gasoline fuel

Y. Zhang and X. Lin, New J. Chem., 2024, 48, 13000 DOI: 10.1039/D4NJ00900B

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